Your browser doesn't support javascript.
loading
MORFAN Syndrome: A Rarity but a Reality!
Roy, Gourab; Sen, Sumit; Poddar, Shreya.
Afiliación
  • Roy G; Department of Dermatology, Institute of Post Graduate Medical Education and Research and SSKM Hospital, Bhowanipore, Kolkata, West Bengal, India.
  • Sen S; Department of Dermatology, Institute of Post Graduate Medical Education and Research and SSKM Hospital, Bhowanipore, Kolkata, West Bengal, India.
  • Poddar S; Department of Dermatology, Institute of Post Graduate Medical Education and Research and SSKM Hospital, Bhowanipore, Kolkata, West Bengal, India.
Indian J Dermatol ; 64(3): 231-234, 2019.
Article en En | MEDLINE | ID: mdl-31148863
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.
Palabras clave

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Indian J Dermatol Año: 2019 Tipo del documento: Article País de afiliación: India

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Indian J Dermatol Año: 2019 Tipo del documento: Article País de afiliación: India