Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Nooh, Deemah M. Bin, Hegazi, Tarek M., Bukhari, Iqbal A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Saudi Medical Journal 2020
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
_version_ 1783643847270596608
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
work_keys_str_mv AT noohdeemahmbin anonychiacongenitaindifferentgenerationsofasinglesaudifamily
AT hegazitarekm anonychiacongenitaindifferentgenerationsofasinglesaudifamily
AT bukhariiqbala anonychiacongenitaindifferentgenerationsofasinglesaudifamily