"Pseudohypoparathyroidism" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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.
| Descriptor ID |
D011547
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| MeSH Number(s) |
C05.116.198.709 C16.320.565.618.815 C18.452.104.709 C18.452.174.766 C18.452.648.618.815
|
| Concept/Terms |
Pseudohypoparathyroidism, Type Ib- Pseudohypoparathyroidism, Type Ib
- Pseudohypoparathyroidisms, Type Ib
- Type Ib Pseudohypoparathyroidism
- Type Ib Pseudohypoparathyroidisms
- PHD1b
- PHD Ib
- PHD Ibs
Pseudohypoparathyroidism, Type Ia- Pseudohypoparathyroidism, Type Ia
- Pseudohypoparathyroidisms, Type Ia
- Type Ia Pseudohypoparathyroidism
- Type Ia Pseudohypoparathyroidisms
- Albright Hereditary Osteodystrophy with Multiple Hormone Resistance
- PHP Ia
|
Below are MeSH descriptors whose meaning is more general than "Pseudohypoparathyroidism".
Below are MeSH descriptors whose meaning is more specific than "Pseudohypoparathyroidism".
This graph shows the total number of publications written about "Pseudohypoparathyroidism" by people in this website by year, and whether "Pseudohypoparathyroidism" was a major or minor topic of these publications.
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Below are the most recent publications written about "Pseudohypoparathyroidism" by people in Profiles.
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A novel mutation adjacent to the switch III domain of G(S alpha) in a patient with pseudohypoparathyroidism. Mol Endocrinol. 1997 Oct; 11(11):1718-27.
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A heterozygous 4-bp deletion mutation in the Gs alpha gene (GNAS1) in a patient with Albright hereditary osteodystrophy. Genomics. 1992 Aug; 13(4):1319-21.
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Thyroid hormone resistance. Annu Rev Med. 1992; 43:363-75.
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Mutations of the Gs alpha-subunit gene in Albright hereditary osteodystrophy detected by denaturing gradient gel electrophoresis. Proc Natl Acad Sci U S A. 1990 Nov; 87(21):8287-90.
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Factors affecting calcium metabolism in disorders of the kidney. Ann Clin Lab Sci. 1981 Jul-Aug; 11(4):327-32.
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Partial gonadotrophin-resistance in pseudohypoparathyroidism. Acta Endocrinol (Copenh). 1978 Jun; 88(2):321-8.