Expanding the phenotypic spectrum of CLCN2-related leucoencephalopathy and ataxia

Abstract Mutations in CLCN2 are a rare cause of autosomal recessive leucoencephalopathy with ataxia and specific imaging abnormalities. Very few cases have been reported to date. Here, we describe the clinical and imaging phenotype of 12 additional CLCN2 patients and expand the known phenotypic spectrum of this disorder. Informed consent was obtained for all patients. Patients underwent either whole-exome sequencing or focused/panel-based sequencing to identify variants. Twelve patients with biallelic CLCN2 variants are described. This includes three novel likely pathogenic missense variants. All patients demonstrated typical MRI changes, including hyperintensity on T2-weighted images in the posterior limbs of the internal capsules, midbrain cerebral peduncles, middle cerebellar peduncles and cerebral white matter. Clinical features included a variable combination of ataxia, headache, spasticity, seizures and other symptoms with a broad range of age of onset. This report is now the largest case series of patients with CLCN2-related leucoencephalopathy and reinforces the finding that, although the imaging appearance is uniform, the phenotypic expression of this disorder is highly heterogeneous. Our findings expand the phenotypic spectrum of CLCN2-related leucoencephalopathy by adding prominent seizures, severe spastic paraplegia and developmental delay.


Graphical Abstract Introduction
Biallelic pathogenic variants in CLCN2 are associated with a rare autosomal recessive leucoencephalopathy with prominent ataxia 1 recently named leucoencephalopathy with ataxia (LKPAT; Online Mendelian Inheritance in Man #615651).][3][4][5][6][7][8][9][10] These observations led to the characterization of a typical phenotype with mild ataxia, variable cognitive impairment, visual impairment from chorioretinopathy or optic atrophy, male infertility and headache. 1Interestingly, all individuals reported to date have remained ambulatory, and current findings suggest very slow disease progression.
MRI reveals a typical pattern of T2 hyperintensity with variable restriction diffusion involving long white matter tracts, particularly the posterior limbs of the internal capsules, midbrain cerebral peduncles and middle cerebellar peduncles, caused by myelin oedema and vacuolization due to impairment in ClC-2 channel-mediated water and ion homeostasis.This imaging pattern is considered very suggestive of this disease. 1owever, due to the very small number of cases reported, it is possible that very mild or atypical forms of this disease go unrecognized, leading to under-diagnosis.Furthermore, most cases of this disease have been observed in European and Asian populations, and few disease-causing variants have been reported so far.
In this study, we describe 12 additional patients with pathogenic or likely pathogenic variants in CLCN2 including three novel missense variants as well as a recurrent nonsense variant associated with a possible founder effect in Brazil.The phenotypic spectrum in this series revealed previously unreported features including pure hereditary spastic paraplegia phenotype, prominent seizures, childhood developmental delay with autism spectrum disorder (ASD) and tremor.Characteristic changes on MRI typical of CLCN2-related leucoencephalopathy were seen in all patients.

Materials and methods
Patients were identified through an active search for CLCN2 pathogenic variants across the entire database of nextgeneration sequencing panels and whole-exome sequencing (WES) of a commercial laboratory (Mendelics Genomic Analysis, São Paulo, SP) and by contacting attending physicians to check for clinical and radiologic findings compatible with leucoencephalopathy (9 patients were obtained by this method).This database contains all patients investigated for numerous reasons, including a suspicion of genetic diseases, screening for cancer susceptibility, among other indications for WES.We also utilized network initiatives on neurogenetic diseases in Brazil, the UK (University College London) and Germany (University Hospital Essen) to search for additional patients with CLCN2-related leucoencephalopathy and ataxia (three patients were obtained by this method).
Informed consent was obtained from the patients in accordance with the Declaration of Helsinki, and the study was approved by the local ethical committee at Universidade Federal do Ceará under the number 5.952.628.DNA was extracted from oral swab samples, and WES was performed on a NovaSeq Illumina platform at Mendelics Genomic Analysis, São Paulo, SP, Brazil.Variants were categorized according to the American College of Medical Genetics guidelines. 11The following transcript was used as reference: NM_004366.6,ENST00000265593.Patients with biallelic pathogenic or probably pathogenic variants were recruited and attending physicians were contacted for clinical information.Clinical history, physical exam, MRI, and additional studies were reviewed for each patient.
Restricted diffusion on MRI was characterized by a visual analysis of lesions in diffusion-weighted image (DWI) and apparent diffusion coefficient (ADC) maps, as hyperintensity and hypointensity, respectively.The high signal on the DWIs suggested diffusion restriction, but unfortunately, we could not properly measure ADC values for all patients, and thus, a T2-shinethrough effect could not be entirely excluded. 12e reviewed the literature for articles in the English language reporting or researching LKPAT associated with CLCN2 published between 1969 and 2023.The search terms 'CLCN2', 'CLC-2 chloride channel', 'CL-2 CL-Channel', 'chloride channel clc-2', 'leucoencephalopathy', 'leucodystrophy', 'white matter disease' and 'lkpat' were used to conduct the search in PubMed, Scopus, Embase, Online Mendelian Inheritance in Man and Cochrane databases.We also searched the reference lists of identified papers.The initial review was conducted in March 2023.
The search yielded 110 articles that were relevant, and 48 articles remained after duplicate identification.We added two articles from one of our references because of their significance to our discussion.After full-text reading, all of them were related to the scope of this review, with 15 case reports and 33 research papers regarding experimental models and molecular aspects of the disease.
Clinical, radiological and molecular data were extracted from reports and case series and used to characterize the clinical profile of LKPAT and compare with the findings of the present series.Molecular and experimental model studies were used to discuss radiologic and molecular findings in light of the most recent developments in the knowledge base of this disease.

Statistical analysis
Data extracted from the participants were summarized using descriptive statistics.Categorical variables were expressed in absolute numbers and percentages.Continuous data were represented in mean values and standard deviation.Comparative statistical analyses were not performed.

Results
We analysed 12 patients from 11 unrelated families (9 from Brazil, 2 from the UK and 1 from Germany), with age of onset varying between 6 months and 62 years (mean 25.95 years; SD 20.26), and among these 12, there were 7 males and 5 females.Most patients were adults (58%).
The most common clinical finding was ataxia in nine patients (75%), which varied from mild to severe cerebellar ataxia.The second most common finding was cognitive decline in five patients (42%), which ranged from cognitive developmental delay and regression to late-onset dementia.Most patients, however, were cognitively normal.Seizures were present in three patients (25%), which were mostly tonic-clonic seizures.Headache was reported by two patients.Prominent pyramidal signs were seen in two patients.In this series, we saw only one patient with self-reported visual impairment.An ophthalmological examination in this patient revealed signs of posterior and anterior uveitis.Visual-evoked potentials and/or digital retinal imaging were performed in two asymptomatic patients and were found to be normal in these patients.
Less common findings were myoclonus, transient ptosis, resting tremor, signs of ASD, psychosis, paroxysmal dyskinaesias and back pain, which were observed in only one patient each.One patient had hemiparesis attributed to a perinatal stroke.Hearing was inventoried clinically and none of the patients reported hearing abnormalities.Audiometry was not routinely performed.Consanguinity was reported in most patients.
MRI revealed symmetric and bilateral T2-hyperintensity involving the posterior limbs of internal capsules, midbrain cerebral peduncles and middle cerebellar peduncles in all patients.Restricted diffusion was suggested by DWI and ADC maps in all 11 cases for which we had access to DWI images, ranging from mild DWI hyperintensity in the splenium of the corpus callosum to diffuse DWI hyperintensity of all long white matter tracts (Fig. 1).Diffusion restriction was more prominent in children than in adult patients.One patient (patient 9) had an area of encephalomalacia surrounded by gliosis in the right temporo-parietal region attributed to a perinatal stroke.In another patient, in addition to the white matter tract involvement previously described, there were also novel findings of grey matter involvement in the form of bilateral putaminal T 2 -hyperintensities with cavitation, involvement of the thalamus and caudate head (Fig. 2).Magnetic resonance findings are summarized in Supplementary Table 1.
Most of the Brazilian patients (eight out of nine patients) had the previously reported c.1709G>A, p.Trp570Ter nonsense pathogenic variant in homozygosity or compound heterozygosity.One of the Brazilian patients had a novel frameshift likely pathogenic variant (p.Leu813Argfs*20) in compound heterozygosis with the c.1709G>A, p.Trp570Ter variant.One British patient had a previously reported missense pathogenic variant (c.1412G>A, p.Arg471His) in homozygosis. 5The other British patient had the novel likely pathogenic p.Leu397Pro variant in homozygosis.We identified three novel likely pathogenic missense variants: c.1015G>C, p.Val339Leu, c.1190T>C, p.Leu397Pro and c.1529C>T, p.Ala510Val (Fig. 3).
The p.Ala510Val variant was present in compound heterozygosis in trans with the c.1709G>A, p.Trp570Ter pathogenic variant in one case and in homozygosis in another.This novel variant has a gnomAD 13 frequency of 0.0000443, with no homozygotes observed.It is predicted to be damaging by computational tools with a DANN 14 score of 0.9993 and a CADD PHRED score of 24.8.It is a conserved residue with a GERP 15 score of 5.1399.Alanine 510 is located in the O transmembrane helical domain.There are no established cut-off values for GERP scores in CLCN2, but a previous study analysing multiple genes found that all pathogenic variants had a GERP score of 2.95 or greater. 16According to the recommendations of the American College of Medical Genetics and Genomics, 11 this variant was classified as likely pathogenic.
The c.1190T>C, p.Leu397Pro novel missense variant has a frequency on gnomAD 13 of 0.00000398.Computational tools predict the variant to be damaging with a DANN 14 score of 0.999 and a CADD PHRED score of 32.It alters a highly conserved residue with a GERP 15 score of 5.73.It was present in one patient in homozygosis.According to the recommendations of the American College of Medical Genetics and Genomics, 11 this variant was classified as likely pathogenic.
The c.1015G>C, p.Val339Leu novel missense variant was identified in the homozygous state in a female patient from Germany.It has a frequency of 0.00001064 (3 heterozygotes), with no homozygotes in gnomAD. 13This variant alters a conserved valine (up to zebrafish) of the J transmembrane domain of the channel and has a CADD PHRED score of 26.5.This variant was classified as of unknown significance but reclassified as likely pathogenic based on the highly concordant brain MRI findings suggestive of LKPAT.
The novel likely pathogenic p.Leu813Argfs*20 frameshift variant leads to a frameshift producing a stop codon.This variant is absent among 141 000 individuals in gnomAD, 13 leads to loss of function, a known mechanism for this disease, and has been found in compound heterozygosis with the previously known p.Trp570Ter variant.It was, therefore, classified as likely pathogenic.
A summary of clinical findings and identified CLCN2 variants with geographical origins may be found in Table 1.Individual case descriptions are available as Supplementary Material.

Discussion
CLCN2 encodes the voltage-gated chloride channel CLC-2, which plays a role in brain ion and water homeostasis. 1ysfunction of this chloride channel is hypothesized to lead to intramyelinic oedema, and therefore, the typical   signal changes on MRI are observed, which characterize CLCN2-related leucoencephalopathy.Variability in phenotype has been reported since the first identification of this disorder, particularly regarding the age of onset.
ClC-2 channels are expressed in the brain mainly in the cell surface of fibrous astrocytes, particularly in the posterior limb of the internal capsules and dense white matter bundles, in astrocytic processes that run parallel or perpendicular to axonal bundles.However, a recent study using cell-type specific CLCN2 knockout mice convincingly shows that loss of CLC-2 from both oligodendrocytes and astrocytes is required to generate a leucodystrophy phenotype (knockout in only astrocytes does not lead to white matter vacuolization), 17 reinforcing the role of multiple glial cell types (the panglial syncytium) in ion and water homeostasis.There is also some expression inside axons and at the axonal surface contacting adaxonal myelin. 1 In perivascular astrocytes, ClC-2 co-localizes with GlialCAM and MLC1.Cerebral white matter is formed mainly by myelinated axons that are involved in impulse conduction.Action potentials are conducted by neuronal depolarization mediated by sodium influx at the nodes of Ranvier, and the osmotic balance is maintained via potassium efflux in myelin-covered paranodal sites.The panglial syncytium is a network of astrocytes, oligodendrocytes and ependymal cells interconnected by gap junctions, which is essential for the disposal of ions and water after the osmolar shift induced by the action potentials.The astrocyte syncytium is particularly responsible for the buffering of rapid volume changes.ClC-2 appears to be involved in the generation of chloride currents necessary for the astrocytic regulatory volume decrease after action potential induced cell swelling, along with MLC1 (megalencephalic leucoencephalopathy with subcortical cysts associated with MLC1).Decreased ClC-2 function in the plasma membrane of astrocytes and olygodendrocytes leads to volume retention, myelinic oedema and vacuolation. 1wo other important proteins, MLC1 and GlialCAM, colocalize with ClC-2 in astrocytic endfeet at the perivascular basal lamina and seem to be part of the same water and ions homeostasis pathway.Both GlialCAM (also known as HEPACAM) and MLC1 are associated with megalencephalic leucoencephalopathy with subcortical cysts (MLC), 18,19 another disease associated with myelin oedema and vacuolation.Different from CLCN2-associated LKPAT, in MLC, most compact white matter tracts such as the corpus callosum, internal capsule, brainstem and cerebellar tracts are spared.MLC1 and GlialCAM are both localized predominantly in distal astrocytic processes, while ClC-2 is more diffusely localized in astrocytes, and this might be related to the predominance of myelinic oedema in long white matter tracts in CLCN2.
Despite the fact that compact white matter tracts are spared in MLC, this disease is more severe than LKPAT.Subcortical white matter oedema in MLC is particularly pronounced, leading to early onset macrocephaly.There is a molecular interaction between ClC-2 and GlialCAM, but the disease caused by loss of function of ClC-2 or GlialCAM is very different, possibly due to a critical role of ion homeostasis in distal astrocytic processes predisposing to early white matter oedema. 20Depienne et al. 1 found only 6 patients with CLCN2 leucoencephalopathy out of a database of 3000 patients with undiagnosed leucoencephalopathy in Amsterdam.They hypothesize that either CLCN2-associated leucoencephalopathy is very rare, or it has a much wider phenotypic variation than previously thought. 1 Our finding of nine new cases in Brazil in a database of ∼60 000 unselected exomes supports this second hypothesis, and screening radiology services for typical MRI findings might reveal an increasingly larger number of patients with very mild or even asymptomatic forms of this disease.
The lack of genotype-phenotype correlation in the small number of case reports to date is reinforced by this report.In this study, Patients 1, 3, 5, 9, 11 and 12 all carried the same homozygous nonsense mutation (p.Trp570Ter), yet there were significant differences not only in the age of onset but also in phenotypic expression between these patients.This variant was present in most cases from Brazil, possibly suggesting a founder effect, although no haplotype analysis was performed to determine ancestry, and therefore, this study is not sufficient to confirm a founder effect.There were 78 heterozygotes for this variant in the database from Mendelics Genomic Analysis, the commercial laboratory where we investigated all Brazilian patients.
The p.Trp570Ter is a loss-of-function variant previously described in the initial paper by Depienne et al. 1 , and this variant has been shown to lead to a downregulation of CLCN2 mRNA and decreased expression of the resulting protein due to nonsense-mediated decay. 1 Many variants described in this gene are loss-of-function variants, either nonsense or frameshift variants. 21e also identified one previously reported CLCN2 missense variant (c.1412G>A, p.Arg471His), one novel likely pathogenic frameshift variant (p.Leu813Argfs*20) and three novel likely pathogenic missense variants, c.1015G>C, p.Val339Leu, c.1190T>C, p.Leu397Pro and c.1529C>T, p.Ala510Val.The novel likely pathogenic p.Leu813Argfs*20 frameshift variant leads to a frameshift producing a stop codon, similarly to other loss-of-function variants described in this gene. 21here are some previously described pathogenic missense variants in this gene.The mechanism by which some of these missense variants might lead to clinical phenotypes has been studied in more detail.These variants are predicted to affect the transmembrane helices B (p.Gly98Arg), N (p.Gly466Glu and p.Arg471His) and O (p.Ala500Val and p.Gly503Arg) of ClC-2 (Fig. 3).In a study of ClC-2 mutants expressed in Xenopus oocytes, none of the mutant ClC-2 channels produced by these variants have elicited activated chloride currents upon hyperpolarization when injected in Xenopus oocytes, and all mutants showed reduced plasma membrane expression, suggesting that the reduced ClC-2 function in these mutants is related to a severely impaired PM expression caused by abnormal trafficking. 22he novel p.Ala510Val missense variant is located in a codon close to the previously reported p.Ala500Val variant, which has been shown to produce CLC-2 channels that were restricted to the endoplasmic reticulum and scarcely expressed in the plasma membrane, possibly due to misfolding caused by the change of conserved hydrophobic amino acids in the transmembrane domains of ClC-2, 1 which are also expected to be affected by the p.Ala510Val variant.Another study on the electrophysiological and biochemical properties of p.Ala500Val mutant ClC-2 channels indicated that this variant does not affect single-channel conductance, but instead changes the gating properties and expression of the channel at the plasmatic membrane, probably due to misfolding and impaired trafficking to plasma membranes. 21It is possible that a similar mechanism occurs with this novel p.Ala510Val variant, as well as with the previously described p.Gly503Arg missense variant. 22he most common clinical features of CLCN2-related leucoencephalopathy reported to date include cerebellar ataxia, visual impairment, headache and male infertility. 1Physical signs include ataxia, tremor, nystagmus and spasticity (Table 2).Uncommon presentations include early onset seizures 7 and paroxysmal dyskinaesia. 3n addition to ataxia, we describe three patients with seizures as a prominent feature, a child with ASD and motor and speech delay, and late-onset patients with fluctuating ataxia and rapid deterioration in spastic paraplegia after injury.These findings might expand the phenotypic spectrum of CLCN2-related leucoencephalopathy and ataxia.
Before the identification of CLCN2-related leucoencephalopathy and ataxia, heterozygous variants in CLCN2 were reported to be a cause of dominant idiopathic generalized epilepsy, [23][24][25][26][27][28] but this finding was later refuted. 29,30Depienne et al. 1 suggested that pathogenic variants in CLCN2 were not associated with epilepsy after none of their six patients and heterozygous asymptomatic relatives had epilepsy.However, two patients with typical LKPAT and seizures were later described in the literature. 7,31In the present series, seizures were reported in one third of patients, suggesting that epilepsy may occur in association with biallelic pathogenic variants in CLCN2.The association of CLCN2 heterozygous variants with epilepsy remains unproved so far.
We reported one patient with spastic paraplegia who became wheelchair-bound at the age of 50, after stabbing wounds to the chest and abdomen.To our knowledge, there are no previous reports of spastic paraplegia leading to loss of ambulation in CLCN2.Interestingly, this patient had no ataxia and no cognitive impairment, presenting as 'pure' hereditary spastic paraplegia.Worsening of white matter diseases after trauma has been previously reported in X-linked adrenoleucodystrophy 32 and in vanishing white matter disease following trauma, systemic infections and even sunbathing. 33This deterioration has been attributed to pro-inflammatory cytokines and blood-brain barrier breakdown in XALD.It is not clear whether the trauma had any causal association with disease worsening in this patient, despite a clear temporal association.
Two siblings were previously reported with an overlap of SPG56-and CLCN2-associated leucoencephalopathy and ataxia, carrying biallelic pathogenic CYP2U1 variants and also biallelic CLCN2 likely pathogenic variants, with azoospermia and MRI compatible with CLCN2, suggesting a true overlap.Severe spastic paraplegia was attributed to SPG56 in these cases. 34,35evelopmental delay with ASD has not been previously reported in LKPAT.A previous study on genetic risk factors for ASD has identified a single identical by descent alteration in CLCN2, 36 but no LKPAT phenotype was reported in association with ASD.Despite the possibility that these psychiatric features are not related to CLCN2 in these patients, the presence of co-occurring ataxia, typical MRI findings and the absence of other variants associated with ASD on WES for one patient suggest that ASD may be part of the LKPAT disease spectrum.Nevertheless, a description of additional cases with these features would be required to definitely conclude that they are part of CLCN2-related disorders.
Although we did not specifically search for male infertility, adult male subjects in this sample had no offspring (involuntary childlessness), suggesting possible infertility.
Despite the highly variable neurological phenotype, all patients had almost identical imaging abnormalities typical of CLCN2-related leucoencephalopathy.The striking DWI features involving long white matter tracts led us to suspect the diagnosis of CLCN2 before WES results in most cases, demonstrating that this finding is a highly suggestive imaging sign.
CLCN2-related leucoencephalopathy should be suspected in patients presenting typical MRI findings, especially symmetric and bilateral T2-hyperintensity involving the posterior limbs of internal capsules, midbrain cerebral peduncles and middle cerebellar peduncles.Other structures commonly involved include the pyramidal tracts in the pons, the central tegmental tracts, cerebellar white matter, corpus callosum and cerebral white matter. 37ome peculiarities of imaging to be highlighted include the presence of restricted diffusion in some affected structures (Fig. 1), usually assigned to intramyelinic oedema caused by small vacuoles and extracellular spaces.The absence of restricted diffusion in most of the cerebral and cerebellar white matter can be related to the existence of large vacuoles and extracellular spaces in these locations, facilitating water movement. 1The reason for this difference in CLCN2-related leucoencephalopathy is not entirely understood.In one case, we identified a novel finding of grey matter involvement in the form of bilateral putaminal T 2 -hyperintensities with cavitation, caudate head and thalamic involvement (Fig. 2).It is not entirely clear whether grey matter involvement is associated with CLCN2 mutations in this case, but WES has been performed, which revealed no other variants of interest.There was no previous history of toxic exposure or other environmental factors.In our cases, there was a trend towards a less prominent involvement of cerebral white matter in adult patients.As intramyelinic oedema can be reversible, there might be some reversal in the cerebral white matter changes with aging in these patients, in the same way that is observed in patients with megalencephalic leucoencephalopathy with subcortical cysts, caused by MLC1 and GlialCAM pathogenic variants that share similar mechanisms in water and ion homeostasis as explained previously.The first description by Depienne et al. 1 also reported more prominent abnormalities in brain white matter among paediatric patients, 1 further reinforcing this possibility of oedema reversal.
Another trend is to notice more widespread areas of restricted diffusion in younger patients (Fig. 1), which can also be explained by differences between small and large vacuoles, since at least in ClC-2 knockout mice, there is a progressive enlargement of the size of vacuoles with age. 38This means that in younger affected individuals, small vacuoles predominate, leading to diffusion restriction, while in older ones, there might be larger vacuoles in which diffusion facilitation can be appreciated.
We found no correlation between the extension of changes on MRI and the severity of clinical presentation.
This study has some limitations.Although it is the largest case series of CLCN2-related LKPAT to date, the number of patients is still too small to draw any genotype-phenotype correlations and to ascertain that some findings, such as ASD and psychosis, are definitely linked to the disease and are not a co-occurrence.Also, we did not perform functional studies to evaluate the biochemical effect of the novel variants reported.Nevertheless, we believe that this case series might draw more attention to the radiologic findings of this disease, leading to an increase in diagnostic suspicion and more cases being reported, especially in different populations from the original European and Asian populations.
This report expands the phenotypic spectrum of CLCN2related leucoencephalopathy by adding prominent seizures, severe spastic paraplegia and developmental delay.These findings highlight the need to screen for CLCN2 mutations when typical imaging features are present.Understanding the components of the ion and water homeostatic pathways might lead to strategies aimed at controlling or reversing myelinic oedema for the treatment of CLCN2-related leucoencephalopathy and related genetic diseases.

Figure 1
Figure 1 MRI findings in patients with CLCN2-related leucoencephalopathy and ataxia.Brain MR from patient 3 (A-L).Axial T2-weighted images (A, D, G, J) demonstrate symmetric bilateral hyperintensity involving the cerebral and cerebellar white matter, posterior limb of internal capsules, midbrain cerebral peduncles, central tegmental tracts (arrowheads in G) and middle cerebellar peduncles.The corresponding DWI (B, E, H, K) and ADC maps (C, F, I, L) suggest restricted diffusion, manifest as DWI hyperintensity and ADC map hypointensity, bilaterally in the subcortical cerebral white matter (arrows in C), posterior limb of internal capsules (arrows in F), midbrain cerebral peduncles (arrows in I) and middle cerebellar peduncles (arrows in L).Brain MR from patient 1 (M-R).Axial T2-weighted images (M, N, P, Q) show symmetric bilateral mild hyperintensity involving the cerebral white matter, which is more prominent in the subcortical region of the right parietal lobe (arrow in M); there is also hyperintensity in the posterior limb of internal capsules, midbrain cerebral peduncles, central tegmental tracts (arrowhead in N) and middle cerebellar peduncles.Also notice the compromise of the splenium of the corpus callosum (arrow in Q).The corresponding ADC maps (O, R) demonstrate hyperintensity in the posterior limb of internal capsules and middle cerebellar peduncles (arrows in O), which represents facilitation (not restriction) of the movement of water molecules.There is some restriction in the splenium of the corpus callosum, shown as hypointensity in the ADC map (arrowhead in R).

Figure 3
Figure 3 Schematics of the ClC-2 chloride channel showing protein domains and reported variants.