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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,...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000Research
2015
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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. |
format | Online Article Text |
id | pubmed-4648218 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | F1000Research |
record_format | MEDLINE/PubMed |
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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