Title of article
RABSON-MENDENHALL SYNDROME: A CASE REPORT
Author/Authors
ALAEI، Mohammad Reza نويسنده MD,Assistant Professor of Pediatric Endocrinology, Shahid Beheshti University of Medical Sciences,Tehran,Iran , , MIRJAVADI، Seyed Alireza نويسنده MD, Resident of Pediatric ,Shahid Beheshti University of Medical Sciences, Tehran,Iran , , SHIARI، Reza نويسنده MD,Ph.D,Assistant Professor of Pediatric Rheumatology,Shahid Beheshti University of Medical Sciences,Tehran,Iran ,
Issue Information
فصلنامه با شماره پیاپی - سال 2010
Pages
4
From page
49
To page
52
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
Journal title
Iranian Journal of Child Neurology (IJCN)
Serial Year
2010
Journal title
Iranian Journal of Child Neurology (IJCN)
Record number
669072
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