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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2019
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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 |
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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 |