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Letter to the Editor - Case Letter
2016:82:6;697-700
doi: 10.4103/0378-6323.190855
PMID: 27643550

Identification of GJB6 gene mutation in an Indian man with Clouston syndrome

Nidheesh Agarwal1 , Pawan Kumar Singh2 , Kalpana Gupta1 , Neerja Gupta2 , Madhulika Kabra2
1 Department of Dermatology, Venereology and Leprosy, Geetanjali Medical College and Hospital, Udaipur, Rajasthan, India
2 Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India

Correspondence Address:
Nidheesh Agarwal
Flat No. 001, Fateh Apartment, New Fatehpura, Udaipur, Rajasthan
India
How to cite this article:
Agarwal N, Singh PK, Gupta K, Gupta N, Kabra M. Identification of GJB6 gene mutation in an Indian man with Clouston syndrome. Indian J Dermatol Venereol Leprol 2016;82:697-700
Copyright: (C)2016 Indian Journal of Dermatology, Venereology, and Leprology

Sir,

Clouston syndrome (MIM 129500), also known as hidrotic ectodermal dysplasia, is a rare autosomal dominant genetic disorder characterized by generalized hypotrichosis, dystrophic nails and hyperkeratotic palms and soles. It is particularly common in the French Canadian population of Southwest Quebec. We present an Indian man with typical clinical features of Clouston syndrome who was found to have a known mutation in the GJB6 gene.

A 45-year-old man presented to the dermatology outpatient department of Geetanjali Medical College and Hospital in Udaipur, Rajasthan, with complaints of excessively thickened skin of the palms and soles. The thickened skin restricted movements of his fingers and disrupted his daily functioning. He gave a history of similar features in one of his children. There was no history of similar lesions in any of his siblings, parents or other family members. None of his family members could be examined.

On examination, the patient was found to have severe hyperkeratosis of the palms and soles which led to clawing of the hands [Figure - 1]. Nails were dystrophic in both hands and feet. The fingernails were thickened, overcurved, discolored [Figure - 2] and associated with tufting of the terminal phalanges [Figure - 1]. Further, the patient had thin and sparse scalp hair [Figure - 3]a. Other hair-bearing regions (eyebrows, eyelids, axillae, pubic region) also had very minimal hair [Figure - 3]b. There was no history of consanguinity, hypohidrosis, abnormal dentition and any hearing or visual complaints. A provisional diagnosis of hidrotic ectodermal dysplasia was made.

Figure 1: Severe hyperkeratosis of palms leading to clawing, along with bulbous terminal phalanges
Figure 2: Thickened, overcurved and discolored finger nails
Figure 3: (a) Thin and sparse scalp hair
Figure 3: (b) Sparse eyebrows, eyelashes and facial hair

A peripheral blood sample was collected in an ethylenediaminetetraacetic acid (EDTA) tube and DNA was isolated by the salting out method.[1] Coding exon 3 of the GJB6 gene was amplified by polymerase chain reaction (PCR) and the amplification checked on 2% agarose gel. Primers used are shown in [Table - 1]. The polymerase chain reaction-amplified product was incubated with exonuclease I and shrimp alkaline phosphatase to remove the unincorporated primers and nucleotides. Bidirectional Sanger deoxyribonucleic acid sequencing was done using ABI Prism BigDye Terminator Cycle sequencing ready reaction kit v3.1 (Applied Biosystems, USA), followed by ethanol/ethylenediamine tetraacetic acid/sodium acetate precipitation. The precipitate was dissolved in 10 µL Hi-Di formamide with denaturation and capillary electrophoresis using an ABI 3130 Genetic Analyzer. Sequencing results were analyzed using Chromas Pro software (http://technelysium.com.au) and compared with the reference sequence of GJB6 in the NCBI database (http://www.ncbi.nlm.nih.gov/). A reported heterozygous missense mutation c. 31G>A (p.G11R) was identified, resulting from a glycine-to-arginine amino acid change [Figure - 4].

Table 1: Primer sequence for connexin 30 (GJB6) gene
Figure 4: A heterozygous c. 31G>A change in the GJB6 gene

Clouston syndrome is a rare genetic disease caused by mutations in connexin genes. Connexins or gap junction proteins are a family of structurally related transmembrane proteins which establish direct cell-to-cell communication and are responsible for the movement of molecules and ions across adjacent cells. They may be classified into three major groups (GJA, GJB and GJC) based on sequence homology. Each combination of connexins has different qualities of permeability highly significant in terms of function. Mutations in connexins result in hereditary peripheral neuropathy, complex conotruncal heart malformations, autosomal dominant forms of cataract and hearing loss. Erythrokeratoderma variabilis, keratitis-ichthyosis-deafness syndrome, Vohwinkel syndrome and Clouston syndrome are cutaneous disorders resulting from connexin mutations.

Mutations in GJB6 gene (and in some cases, GJA1 and GJB2 genes) are responsible for Clouston syndrome. To date, five different mutations have been reported in GJB6 gene with phenotypic features of Clouston syndrome. Mutations p.G11R and p.A88V have been described by Lamartine et al. in multiple ethnic populations, p.V37E by Smith et al. in Scottish patients and p.D50N by Baris et al. in Israeli patients.2-4 Recently, Liu et al. have found that the combination of a novel mutation N14S in GJB6 and a mutation F191L in GJB2 played a pathogenic role in Clouston syndrome.[5] Mutations in GJA1 (p.V41L) and an R127H heterozygous variants of GJB2 have also been found responsible for Clouston syndrome.[6] Out of all these, p.G11R is the most commonly reported mutation, seen in the French Canadian population as well as in many other ethnic populations of the world.

We could find only two previous reports of Clouston syndrome in Indians. One was of a large Gujarati family with 41 affected individuals spanning five generations, but genetic mutations were not explored in this family.[7] The other report described a p.A88V mutation detected by Lamartine et al. in a patient of Indian ethnicity.[2]

Our patient presented with typical features, and since he denied any similar features in his parents, it was probably a sporadic case. The mutation detected, c. 31G>A (p.G11R) in the GJB6 gene, is a known mutation.

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has given his consent for his images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

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