Rabson-Mendenhall syndrome: a case report
IJCN-Iranian Journal of Child Neurology. 2010; 4 (1): 49-52
en Inglés
| IMEMR
| ID: emr-123718
ABSTRACT
Rabson-Mendenhall syndrome is a rare genetic disorder characterized by growth retardation, dysmorphisms, lack of subcutaneous fat, acanthosis nigricans, enlarged genitalia, hirsutism, dysplastic dentition, coarse facial features, paradoxical fasting hypoglycemia, postprandial hyperglycemia, extreme hyperinsulinemia and pineal hyperplasia. Herein, we described a 10-year-old girl with physical features of the Rabson-Mendenhall syndrome that was presented with polyuria. To our knowledge, this is the first report of the Rabson-Mendenhall syndrome from Iran
Buscar en Google
Índice:
IMEMR (Mediterraneo Oriental)
Asunto principal:
Poliuria
/
Resistencia a la Insulina
/
Clítoris
/
Diabetes Mellitus
/
Hirsutismo
Tipo de estudio:
Informe de Casos
Límite:
Femenino
/
Humanos
Idioma:
Inglés
Revista:
Iran. J. Child Neurol.
Año:
2010
Similares
MEDLINE
...
LILACS
LIS