Literature DB >> 15738613

Rabson-Mendenhall syndrome.

Sarita Kumar1, Milind S Tullu, Mamta N Muranjan, Jaishree R Kamat.   

Abstract

Rabson-Mendenhall syndrome is characterized by growth retardation, dysmorphisms, lack of subcutaneous fat, acanthosis nigricans, enlarged genitalia, hirsutism, premature and dysplastic dentition, coarse facial features, paradoxical fasting hypoglycemia and post-prandial hyperglycemia, extreme hyperinsulinemia and pineal hyperplasia. We describe a six-month-old female child with physical features suggestive of the Rabson-Mendenhall syndrome. The child also had medullary nephrocalcinosis.

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Year:  2005        PMID: 15738613

Source DB:  PubMed          Journal:  Indian J Med Sci        ISSN: 0019-5359


  4 in total

Review 1.  Rabson-Mendenhall syndrome: two case reports and a brief review of the literature.

Authors:  Renuka J Bathi; Sameena Parveen; Sunil Mutalik; Reema Rao
Journal:  Odontology       Date:  2010-02-16       Impact factor: 2.634

2.  Rabson-Mendenhall syndrome: medullary sponge kidney, a new component.

Authors:  Andrew M Harris; Bryan Hall; Vesna M Kriss; John L Fowlkes; Stefan G Kiessling
Journal:  Pediatr Nephrol       Date:  2007-09-12       Impact factor: 3.714

3.  Renal manifestations of severe Rabson-Mendenhall syndrome: a case report.

Authors:  Yih Harng Chong; Barry J Taylor; Benjamin J Wheeler
Journal:  J Diabetes Metab Disord       Date:  2013-01-22

4.  Rabson-mendenhall syndrome.

Authors:  Iffat Hassan; Hinah Altaf; Atiya Yaseen
Journal:  Indian J Dermatol       Date:  2014-11       Impact factor: 1.494

  4 in total

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