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Published in 2021 at "Endocrine"
DOI: 10.1007/s12020-021-02821-y
Abstract: Progressive osseous heteroplasia (POH), a genetic disorder, is associated with Albright’s hereditary osteodystrophy (AHO), pseudohypoparathyroidism, and primary osteoma cutis and has common features of superficial ossification and GNAS-inactivating mutations. Disorders due to GNAS-inactivating mutations are…
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Keywords:
pth;
overlap syndrome;
tsh resistance;
early childhood ... See more keywords