Monilethrix with Holt-Oram Syndrome: Case Report of a Rare Association

Congenital hypotrichosis may be due to a number of causes and may have multiple systemic associations. A child born of second-degree consanguineous marriage was found to have monilethrix as the cause of congenital hypotrichosis. A detailed systemic evaluation in the child revealed atrial septal defe...

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Autores principales: Shah, Vivek, Tharini, GK, Manoharan, K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4387697/
https://www.ncbi.nlm.nih.gov/pubmed/25878448
http://dx.doi.org/10.4103/0974-7753.153455
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author Shah, Vivek
Tharini, GK
Manoharan, K
author_facet Shah, Vivek
Tharini, GK
Manoharan, K
author_sort Shah, Vivek
collection PubMed
description Congenital hypotrichosis may be due to a number of causes and may have multiple systemic associations. A child born of second-degree consanguineous marriage was found to have monilethrix as the cause of congenital hypotrichosis. A detailed systemic evaluation in the child revealed atrial septal defect and a hypoplastic right thumb leading to a diagnosis of coexisting Holt-Oram syndrome.
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spelling pubmed-43876972015-04-15 Monilethrix with Holt-Oram Syndrome: Case Report of a Rare Association Shah, Vivek Tharini, GK Manoharan, K Int J Trichology Case Report Congenital hypotrichosis may be due to a number of causes and may have multiple systemic associations. A child born of second-degree consanguineous marriage was found to have monilethrix as the cause of congenital hypotrichosis. A detailed systemic evaluation in the child revealed atrial septal defect and a hypoplastic right thumb leading to a diagnosis of coexisting Holt-Oram syndrome. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4387697/ /pubmed/25878448 http://dx.doi.org/10.4103/0974-7753.153455 Text en Copyright: © International Journal of Trichology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Shah, Vivek
Tharini, GK
Manoharan, K
Monilethrix with Holt-Oram Syndrome: Case Report of a Rare Association
title Monilethrix with Holt-Oram Syndrome: Case Report of a Rare Association
title_full Monilethrix with Holt-Oram Syndrome: Case Report of a Rare Association
title_fullStr Monilethrix with Holt-Oram Syndrome: Case Report of a Rare Association
title_full_unstemmed Monilethrix with Holt-Oram Syndrome: Case Report of a Rare Association
title_short Monilethrix with Holt-Oram Syndrome: Case Report of a Rare Association
title_sort monilethrix with holt-oram syndrome: case report of a rare association
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4387697/
https://www.ncbi.nlm.nih.gov/pubmed/25878448
http://dx.doi.org/10.4103/0974-7753.153455
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AT manoharank monilethrixwithholtoramsyndromecasereportofarareassociation

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