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PubMed · 15738613

Rabson-Mendenhall syndrome.

Sarita Kumar·Milind S Tullu·Mamta N Muranjan·Jaishree R Kamat
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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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Abnormalities, MultipleAcanthosis NigricansConsanguinityDiabetes MellitusDiabetic KetoacidosisFailure to ThriveFemaleGrowth DisordersHirsutismHumansInfantInsulin ResistanceOdontodysplasiaSyndromeCase ReportsJournal Article

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Sarita Kumar, Milind S Tullu, Mamta N Muranjan, Jaishree R Kamat. 2005. Rabson-Mendenhall syndrome.. https://pubmed.ncbi.nlm.nih.gov/15738613/

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