Pseudohypoparathyroidism
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.
Year introduced: 1965(1963)
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Subheadings:
Tree Number(s): C05.116.198.709, C16.320.565.618.815, C18.452.104.709, C18.452.174.766, C18.452.648.618.815
MeSH Unique ID: D011547
Entry Terms:
- Pseudohypoparathyroidisms
- Pseudohypoparathyroidism, Type Ib
- Pseudohypoparathyroidisms, Type Ib
- Type Ib Pseudohypoparathyroidism
- Type Ib Pseudohypoparathyroidisms
- PHD Ib
- PHD1b
- Pseudohypoparathyroidism Type 1B
- Pseudohypoparathyroidism Type 1Bs
- Pseudohypoparathyroidism, Type Ia
- Pseudohypoparathyroidisms, Type Ia
- Type Ia Pseudohypoparathyroidism
- Type Ia Pseudohypoparathyroidisms
- PHPIa
- Albright Hereditary Osteodystrophy
- Hereditary Osteodystrophy, Albright
- Osteodystrophy, Albright Hereditary
- PHP Ia
- Albright Hereditary Osteodystrophy with Multiple Hormone Resistance
See Also: