Rabson-Mendenhall syndrome

(rab´sәn men´dәn-hawl) 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.
Found on http://www.encyclo.co.uk/local/21001
No exact match found