Indian Journal of Dermatology (Jan 2019)

MORFAN syndrome: A rarity but a reality!

  • Gourab Roy,
  • Sumit Sen,
  • Shreya Poddar

DOI
https://doi.org/10.4103/ijd.IJD_160_19
Journal volume & issue
Vol. 64, no. 3
pp. 231 – 234

Abstract

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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.

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