 Pseudohypoparathyroidism
"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
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| 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
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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.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2001 | 1 | 0 | 1 | | 2022 | 1 | 0 | 1 |
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Below are the most recent publications written about "Pseudohypoparathyroidism" by people in Profiles.
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Shelkowitz E, Chan CM, Jones T, Nakano SJ, Meeks NJL. A novel GNAS variant presents with disorders of GNAS inactivation and cardiomyopathy. Am J Med Genet A. 2022 07; 188(7):2147-2152.
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Perez KM, Lee EB, Kahanda S, Duis J, Reyes M, J?ppner H, Shoemaker AH. Cognitive and behavioral phenotype of children with pseudohypoparathyroidism type 1A. Am J Med Genet A. 2018 02; 176(2):283-289.
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Miyake A, Inoue Y, Omori M, Yonei T, Sato T. [Pseudohypoparathyroidism presenting laryngospasm]. Nihon Naika Gakkai Zasshi. 2001 Nov 10; 90(11):2282-3.
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