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Case Report: Whole exome sequencing helps in accurate molecular diagnosis in siblings with a rare co-occurrence of paternally inherited 22q12 duplication and autosomal recessive non-syndromic ichthyosis.

Lamellar ichthyosis (LI), considered an autosomal recessive monogenic genodermatosis, has an incidence of approximately 1 in 250,000. Usually associated with mutations in the transglutaminase gene ( TGM1), mutations in six other genes have, less frequently, been shown to be causative. Two siblings,...

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Autores principales: Gupta, Aayush, Sharma, Yugal, Deo, Kirti, Vellarikkal, Shamsudheen, Jayarajan, Rijith, Dixit, Vishal, Verma, Ankit, Scaria, Vinod, Sivasubbu, Sridhar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000Research 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4648218/
https://www.ncbi.nlm.nih.gov/pubmed/26594337
http://dx.doi.org/10.12688/f1000research.6779.1
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author Gupta, Aayush
Sharma, Yugal
Deo, Kirti
Vellarikkal, Shamsudheen
Jayarajan, Rijith
Dixit, Vishal
Verma, Ankit
Scaria, Vinod
Sivasubbu, Sridhar
author_facet Gupta, Aayush
Sharma, Yugal
Deo, Kirti
Vellarikkal, Shamsudheen
Jayarajan, Rijith
Dixit, Vishal
Verma, Ankit
Scaria, Vinod
Sivasubbu, Sridhar
author_sort Gupta, Aayush
collection PubMed
description Lamellar ichthyosis (LI), considered an autosomal recessive monogenic genodermatosis, has an incidence of approximately 1 in 250,000. Usually associated with mutations in the transglutaminase gene ( TGM1), mutations in six other genes have, less frequently, been shown to be causative. Two siblings, born in a collodion membrane, presented with fish like scales all over the body. Karyotyping revealed duplication of the chromosome arm on 22q12+ in the father and two siblings. Whole exome sequencing revealed a homozygous p.Gly218Ser variation in TGM1; a variation reported earlier in an isolated Finnish population in association with autosomal recessive non-syndromic ichthyosis. This concurrence of a potentially benign 22q12+ duplication and LI, both rare individually, is reported here likely for the first time.
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spelling pubmed-46482182015-11-20 Case Report: Whole exome sequencing helps in accurate molecular diagnosis in siblings with a rare co-occurrence of paternally inherited 22q12 duplication and autosomal recessive non-syndromic ichthyosis. Gupta, Aayush Sharma, Yugal Deo, Kirti Vellarikkal, Shamsudheen Jayarajan, Rijith Dixit, Vishal Verma, Ankit Scaria, Vinod Sivasubbu, Sridhar F1000Res Case Report Lamellar ichthyosis (LI), considered an autosomal recessive monogenic genodermatosis, has an incidence of approximately 1 in 250,000. Usually associated with mutations in the transglutaminase gene ( TGM1), mutations in six other genes have, less frequently, been shown to be causative. Two siblings, born in a collodion membrane, presented with fish like scales all over the body. Karyotyping revealed duplication of the chromosome arm on 22q12+ in the father and two siblings. Whole exome sequencing revealed a homozygous p.Gly218Ser variation in TGM1; a variation reported earlier in an isolated Finnish population in association with autosomal recessive non-syndromic ichthyosis. This concurrence of a potentially benign 22q12+ duplication and LI, both rare individually, is reported here likely for the first time. F1000Research 2015-07-31 /pmc/articles/PMC4648218/ /pubmed/26594337 http://dx.doi.org/10.12688/f1000research.6779.1 Text en Copyright: © 2015 Gupta A et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Gupta, Aayush
Sharma, Yugal
Deo, Kirti
Vellarikkal, Shamsudheen
Jayarajan, Rijith
Dixit, Vishal
Verma, Ankit
Scaria, Vinod
Sivasubbu, Sridhar
Case Report: Whole exome sequencing helps in accurate molecular diagnosis in siblings with a rare co-occurrence of paternally inherited 22q12 duplication and autosomal recessive non-syndromic ichthyosis.
title Case Report: Whole exome sequencing helps in accurate molecular diagnosis in siblings with a rare co-occurrence of paternally inherited 22q12 duplication and autosomal recessive non-syndromic ichthyosis.
title_full Case Report: Whole exome sequencing helps in accurate molecular diagnosis in siblings with a rare co-occurrence of paternally inherited 22q12 duplication and autosomal recessive non-syndromic ichthyosis.
title_fullStr Case Report: Whole exome sequencing helps in accurate molecular diagnosis in siblings with a rare co-occurrence of paternally inherited 22q12 duplication and autosomal recessive non-syndromic ichthyosis.
title_full_unstemmed Case Report: Whole exome sequencing helps in accurate molecular diagnosis in siblings with a rare co-occurrence of paternally inherited 22q12 duplication and autosomal recessive non-syndromic ichthyosis.
title_short Case Report: Whole exome sequencing helps in accurate molecular diagnosis in siblings with a rare co-occurrence of paternally inherited 22q12 duplication and autosomal recessive non-syndromic ichthyosis.
title_sort case report: whole exome sequencing helps in accurate molecular diagnosis in siblings with a rare co-occurrence of paternally inherited 22q12 duplication and autosomal recessive non-syndromic ichthyosis.
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4648218/
https://www.ncbi.nlm.nih.gov/pubmed/26594337
http://dx.doi.org/10.12688/f1000research.6779.1
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