A hereditary syndrome clinically similar to HYPOPARATHYROIDISM. It is characterized by HYPOCALCEMIA; HYPERPHOSPHATEMIA; and associated skeletal development impairment and caused by failure of response to PARATHYROID HORMONE rather than deficiencies. A severe form with resistance to multiple hormones is referred to as Type 1a and is associated with maternal mutant allele of the ALPHA CHAIN OF STIMULATORY G PROTEIN.
Also Known As:
Albright Hereditary Osteodystrophy with Multiple Hormone Resistance; PHD Ib; PHD1b; PHP Ia; Pseudohypoparathyroidism Type 1B; Pseudohypoparathyroidism, Type Ia; Pseudohypoparathyroidism, Type Ib; Hereditary Osteodystrophy, Albright; Osteodystrophy, Albright Hereditary; Pseudohypoparathyroidism Type 1Bs; Pseudohypoparathyroidisms; Pseudohypoparathyroidisms, Type Ia; Pseudohypoparathyroidisms, Type Ib; Type Ia Pseudohypoparathyroidism; Type Ia Pseudohypoparathyroidisms; Type Ib Pseudohypoparathyroidism; Type Ib Pseudohypoparathyroidisms; Albright Hereditary Osteodystrophy; PHPIa