Ontology highlight
ABSTRACT:
SUBMITTER: Mannava P
PROVIDER: S-EPMC4310850 | biostudies-other | 2015 Jan
REPOSITORIES: biostudies-other
Mannava Prasanthi P Masood Afshan A Devi Ambika K AK
Indian journal of clinical biochemistry : IJCB 20140715 1
Albright hereditary osteodystrophy (AHO) is a rare hereditary metabolic disorder that may or may not be associated with resistance to parathyroid hormone (pseudohypoparathyroidism) or other hormones. The disorder is commonly characterized by a constellation of dysmorphic physical features and with biochemical levels that demonstrate hypocalcaemia and hyperphosphatemia. We report here a clinical case of a 14 year old male with AHO and we discuss his clinical features, radiographic and laboratory ...[more]