Rabson-Mendenhall syndrome
- Rabson-Mendenhall syndrome
- a rare syndrome seen in children, characterized by a mutation or other defect in an insulin receptor gene, with severe insulin resistance and acanthosis nigricans as well as thick hair, abnormalities of teeth and nails, and hyperplasia of the pineal gland.
Medical dictionary.
2011.
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Rabson-Mendenhall syndrome — Infobox Disease Name = PAGENAME Caption = DiseasesDB = ICD10 = ICD9 = ICDO = OMIM = 262190 MedlinePlus = MeshName = MeshNumber = Rabson Mendenhall syndrome is a rare insulin receptor disordercite journal |author=Kasuga M, Kadowaki T… … Wikipedia
Rabson-Mendenhall syndrome — Rab·son Men·den·hall syndrome (rabґsən menґdən hawl) [S.M. Rabson, American physician, 20th century; E.N. Mendenhall, American physician, 20th century] see under syndrome … Medical dictionary
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