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Anonychia congenita in different generations of a single Saudi family
Anonychia refers to the absence of nail plates owing to an autosomal dominant or recessive inheritance. Congenital anonychia is a rare condition that may be associated with other ectodermal or mesodermal malformations like epidermolysis bullosa, (deafness, onychodystrophy, osteodystrophy, and mental...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Saudi Medical Journal
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7841626/ https://www.ncbi.nlm.nih.gov/pubmed/32020155 http://dx.doi.org/10.15537/smj.2020.2.24884 |
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author | Nooh, Deemah M. Bin Hegazi, Tarek M. Bukhari, Iqbal A. |
author_facet | Nooh, Deemah M. Bin Hegazi, Tarek M. Bukhari, Iqbal A. |
author_sort | Nooh, Deemah M. Bin |
collection | PubMed |
description | Anonychia refers to the absence of nail plates owing to an autosomal dominant or recessive inheritance. Congenital anonychia is a rare condition that may be associated with other ectodermal or mesodermal malformations like epidermolysis bullosa, (deafness, onychodystrophy, osteodystrophy, and mental retardation) syndrome and Iso-Kikuchi syndrome. Here, we report 3 cases with anonychia congenita appearing in different generations of a single family in Kingdom of Saudi Arabia. |
format | Online Article Text |
id | pubmed-7841626 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Saudi Medical Journal |
record_format | MEDLINE/PubMed |
spelling | pubmed-78416262021-03-08 Anonychia congenita in different generations of a single Saudi family Nooh, Deemah M. Bin Hegazi, Tarek M. Bukhari, Iqbal A. Saudi Med J Case Report Anonychia refers to the absence of nail plates owing to an autosomal dominant or recessive inheritance. Congenital anonychia is a rare condition that may be associated with other ectodermal or mesodermal malformations like epidermolysis bullosa, (deafness, onychodystrophy, osteodystrophy, and mental retardation) syndrome and Iso-Kikuchi syndrome. Here, we report 3 cases with anonychia congenita appearing in different generations of a single family in Kingdom of Saudi Arabia. Saudi Medical Journal 2020-02 /pmc/articles/PMC7841626/ /pubmed/32020155 http://dx.doi.org/10.15537/smj.2020.2.24884 Text en Copyright: © Saudi Medical Journal http://creativecommons.org/licenses/by-nc This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial License (CC BY-NC), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Nooh, Deemah M. Bin Hegazi, Tarek M. Bukhari, Iqbal A. Anonychia congenita in different generations of a single Saudi family |
title | Anonychia congenita in different generations of a single Saudi family |
title_full | Anonychia congenita in different generations of a single Saudi family |
title_fullStr | Anonychia congenita in different generations of a single Saudi family |
title_full_unstemmed | Anonychia congenita in different generations of a single Saudi family |
title_short | Anonychia congenita in different generations of a single Saudi family |
title_sort | anonychia congenita in different generations of a single saudi family |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7841626/ https://www.ncbi.nlm.nih.gov/pubmed/32020155 http://dx.doi.org/10.15537/smj.2020.2.24884 |
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