1.
Indian J Dermatol
; 59(6): 633, 2014 Nov.
Artículo
en Inglés
| MEDLINE
| ID: mdl-25484423
RESUMEN
Rabson-Mendenhall syndrome (RMS) is a rare genetic disorder characterized by growth retardation, dysmorphisms, lack of subcutaneous fat, acanthosis nigricans, enlarged genitalia, hirsutism, dysplastic dentition, coarse facial features, abnormal glucose homeostasis, hyperinsulinemia and pineal hyperplasia. Herein, we describe a 13-year-old girl with physical features of RMS who presented to us on account of acanthosis nigricans.
2.
Indian J Dermatol Venereol Leprol
; 79(6): 813-6, 2013.
Artículo
en Inglés
| MEDLINE
| ID: mdl-24177617