Rabson-Mendenhall Syndrome

Rabson-Mendenhall syndrome (RMS) is a rare genetic disorder characterized by growth retardation, dysmorphisms, lack of subcutaneous fat, acanthosis nigricans, enlarged genitalia, hirsutism, dysplastic dentition, coarse facial features, abnormal glucose homeostasis, hyperinsulinemia and pineal hyperp...

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Detalles Bibliográficos
Autores principales: Hassan, Iffat, Altaf, Hinah, Yaseen, Atiya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
E-IJD Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4248531/
https://www.ncbi.nlm.nih.gov/pubmed/25484423
http://dx.doi.org/10.4103/0019-5154.143579
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author Hassan, Iffat
Altaf, Hinah
Yaseen, Atiya
author_facet Hassan, Iffat
Altaf, Hinah
Yaseen, Atiya
author_sort Hassan, Iffat
collection PubMed
description Rabson-Mendenhall syndrome (RMS) is a rare genetic disorder characterized by growth retardation, dysmorphisms, lack of subcutaneous fat, acanthosis nigricans, enlarged genitalia, hirsutism, dysplastic dentition, coarse facial features, abnormal glucose homeostasis, hyperinsulinemia and pineal hyperplasia. Herein, we describe a 13-year-old girl with physical features of RMS who presented to us on account of acanthosis nigricans.
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spelling pubmed-42485312014-12-05 Rabson-Mendenhall Syndrome Hassan, Iffat Altaf, Hinah Yaseen, Atiya Indian J Dermatol E-IJD Case Report Rabson-Mendenhall syndrome (RMS) is a rare genetic disorder characterized by growth retardation, dysmorphisms, lack of subcutaneous fat, acanthosis nigricans, enlarged genitalia, hirsutism, dysplastic dentition, coarse facial features, abnormal glucose homeostasis, hyperinsulinemia and pineal hyperplasia. Herein, we describe a 13-year-old girl with physical features of RMS who presented to us on account of acanthosis nigricans. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4248531/ /pubmed/25484423 http://dx.doi.org/10.4103/0019-5154.143579 Text en Copyright: © Indian Journal of Dermatology 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 E-IJD Case Report
Hassan, Iffat
Altaf, Hinah
Yaseen, Atiya
Rabson-Mendenhall Syndrome
title Rabson-Mendenhall Syndrome
title_full Rabson-Mendenhall Syndrome
title_fullStr Rabson-Mendenhall Syndrome
title_full_unstemmed Rabson-Mendenhall Syndrome
title_short Rabson-Mendenhall Syndrome
title_sort rabson-mendenhall syndrome
topic E-IJD Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4248531/
https://www.ncbi.nlm.nih.gov/pubmed/25484423
http://dx.doi.org/10.4103/0019-5154.143579
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