Reza ALAEI, Mohammad and Alireza MIRJAVADI, Seyed and SHIARI, Reza (2010) Rabson-Mendenhall Syndrome: A Case Report. Iranian Journal of Child Neurology, 4 (1). pp. 49-52.
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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.
| Item Type: | Article |
|---|---|
| Subjects: | South Asian Archive > Medical Science |
| Depositing User: | Unnamed user with email support@southasianarchive.com |
| Date Deposited: | 31 Mar 2023 06:50 |
| Last Modified: | 20 Dec 2024 09:02 |
| URI: | http://press.eprintscholarpress.in/id/eprint/197 |
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