 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 condition clinically resembling HYPOPARATHYROIDISM, but caused by failure of response to rather than deficiency of parathyroid hormones. It is characterized by hypocalcemia and hyperphosphatemia, and is commonly associated with short stature, obesity, short metacarpals, and ectopic calcification. (Dorland, 27th ed)
| Descriptor ID |
D011547
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| MeSH Number(s) |
C05.116.198.709 C16.320.565.618.815 C18.452.174.766 C18.452.648.618.815
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| Concept/Terms |
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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 |
|---|
| 1981 | 0 | 1 | 1 | | 1990 | 1 | 0 | 1 | | 1992 | 2 | 0 | 2 | | 1997 | 1 | 0 | 1 |
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Below are the most recent publications written about "Pseudohypoparathyroidism" by people in Profiles.
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Warner DR, Gejman PV, Collins RM, Weinstein LS. 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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Weinstein LS, Gejman PV, de Mazancourt P, American N, Spiegel AM. 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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Weiss RE, Refetoff S. Thyroid hormone resistance. Annu Rev Med. 1992; 43:363-75.
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Weinstein LS, Gejman PV, Friedman E, Kadowaki T, Collins RM, Gershon ES, Spiegel AM. 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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Favus MJ. Factors affecting calcium metabolism in disorders of the kidney. Ann Clin Lab Sci. 1981 Jul-Aug; 11(4):327-32.
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