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MORFAN syndrome: A rarity but a reality!
- 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]
- Subjects :
- *ADENOCARCINOMA
*AXILLA
*ENDOCRINE diseases
*GROIN
*HYPERINSULINISM
*INSULIN resistance
*LAURENCE-Moon-Biedl syndrome
*MARFAN syndrome
*MELANOSIS
*PEOPLE with intellectual disabilities
*NECK
*OBESITY
*RARE diseases
*GASTROINTESTINAL tumors
*ALSTROM syndrome
*LIPODYSTROPHY
*HYPERPIGMENTATION
*DONOHUE syndrome
Subjects
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