"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.
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Year | Major Topic | Minor Topic | Total |
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1997 | 1 | 0 | 1 |
2006 | 1 | 0 | 1 |
2023 | 1 | 0 | 1 |
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Below are the most recent publications written about "Pseudohypoparathyroidism" by people in Profiles.
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Intrafamilial phenotypic heterogeneity in siblings with pseudohypoparathyroidism 1B due to maternal STX16 deletion. J Pediatr Endocrinol Metab. 2024 Jan 29; 37(1):84-89.
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Pseudohypoparathyroidism type 1a with congenital hypothyroidism. J Pediatr Endocrinol Metab. 2006 Aug; 19(8):1049-52.
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Deletion of chromosome 22q11 and pseudohypoparathyroidism. Am J Med Genet. 1997 Oct 03; 72(1):63-5.
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Synthetic human parathyroid hormone-(1-34) for the study of pseudohypoparathyroidism. J Clin Endocrinol Metab. 1988 Nov; 67(5):964-72.
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A case of pseudohypoparathyroidism type 1 associated with gonadotropin resistance and hypercalcitoninaemia. Jpn J Med. 1988 May; 27(2):207-10.