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MORFAN syndrome: A rarity but a reality!

Authors :
Roy, Gourab
Sen, Sumit
Poddar, Shreya
Source :
Indian Journal of Dermatology. May/Jun2019, Vol. 64 Issue 3, p231-234. 4p.
Publication Year :
2019

Abstract

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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00195154
Volume :
64
Issue :
3
Database :
Academic Search Index
Journal :
Indian Journal of Dermatology
Publication Type :
Academic Journal
Accession number :
136735119
Full Text :
https://doi.org/10.4103/ijd.IJD_160_19