Cargando…

MORFAN Syndrome: A Rarity but a Reality!

Acanthosis nigricans (AN) describes clinically hyperpigmented skin, which most commonly affects the flexural areas such as axilla, groin and neck. It is usually a benign condition associated with obesity, insulin resistance, and hyperinsulinemia; endocrinopathy; or malignancy, in particular, gastroi...

Descripción completa

Detalles Bibliográficos
Autores principales: Roy, Gourab, Sen, Sumit, Poddar, Shreya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6537694/
https://www.ncbi.nlm.nih.gov/pubmed/31148863
http://dx.doi.org/10.4103/ijd.IJD_160_19
_version_ 1783422067921649664
author Roy, Gourab
Sen, Sumit
Poddar, Shreya
author_facet Roy, Gourab
Sen, Sumit
Poddar, Shreya
author_sort Roy, Gourab
collection PubMed
description Acanthosis nigricans (AN) describes clinically hyperpigmented skin, which most commonly affects the flexural areas such as axilla, groin and neck. It is usually a benign condition associated with obesity, insulin resistance, and hyperinsulinemia; endocrinopathy; or malignancy, in particular, gastrointestinal adenocarcinoma. It can also occur in association with various genetic syndromes involving various organ systems. Few such known syndromes are Berardinelli-Seip syndrome, Alström syndrome, Leprechaunism, and Bardet-Biedl syndrome. MORFAN syndrome, which associates mild mental retardation, pre- and post-natal overgrowth, remarkable facies and diffuse and widespread AN, is a rare entity.
format Online
Article
Text
id pubmed-6537694
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Wolters Kluwer - Medknow
record_format MEDLINE/PubMed
spelling pubmed-65376942019-05-30 MORFAN Syndrome: A Rarity but a Reality! Roy, Gourab Sen, Sumit Poddar, Shreya Indian J Dermatol Case Report Acanthosis nigricans (AN) describes clinically hyperpigmented skin, which most commonly affects the flexural areas such as axilla, groin and neck. It is usually a benign condition associated with obesity, insulin resistance, and hyperinsulinemia; endocrinopathy; or malignancy, in particular, gastrointestinal adenocarcinoma. It can also occur in association with various genetic syndromes involving various organ systems. Few such known syndromes are Berardinelli-Seip syndrome, Alström syndrome, Leprechaunism, and Bardet-Biedl syndrome. MORFAN syndrome, which associates mild mental retardation, pre- and post-natal overgrowth, remarkable facies and diffuse and widespread AN, is a rare entity. Wolters Kluwer - Medknow 2019 /pmc/articles/PMC6537694/ /pubmed/31148863 http://dx.doi.org/10.4103/ijd.IJD_160_19 Text en Copyright: © 2019 Indian Journal of Dermatology http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Roy, Gourab
Sen, Sumit
Poddar, Shreya
MORFAN Syndrome: A Rarity but a Reality!
title MORFAN Syndrome: A Rarity but a Reality!
title_full MORFAN Syndrome: A Rarity but a Reality!
title_fullStr MORFAN Syndrome: A Rarity but a Reality!
title_full_unstemmed MORFAN Syndrome: A Rarity but a Reality!
title_short MORFAN Syndrome: A Rarity but a Reality!
title_sort morfan syndrome: a rarity but a reality!
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6537694/
https://www.ncbi.nlm.nih.gov/pubmed/31148863
http://dx.doi.org/10.4103/ijd.IJD_160_19
work_keys_str_mv AT roygourab morfansyndromeararitybutareality
AT sensumit morfansyndromeararitybutareality
AT poddarshreya morfansyndromeararitybutareality