 Hypoparathyroidism
"Hypoparathyroidism" 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 condition caused by a deficiency of PARATHYROID HORMONE (or PTH). It is characterized by HYPOCALCEMIA and hyperphosphatemia. Hypocalcemia leads to TETANY. The acquired form is due to removal or injuries to the PARATHYROID GLANDS. The congenital form is due to mutations of genes, such as TBX1; (see DIGEORGE SYNDROME); CASR encoding CALCIUM-SENSING RECEPTOR; or PTH encoding parathyroid hormone.
| Descriptor ID |
D007011
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| MeSH Number(s) |
C19.642.482
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Hypoparathyroidism".
Below are MeSH descriptors whose meaning is more specific than "Hypoparathyroidism".
This graph shows the total number of publications written about "Hypoparathyroidism" by people in this website by year, and whether "Hypoparathyroidism" 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 |
|---|
| 2012 | 1 | 0 | 1 | | 2017 | 1 | 0 | 1 | | 2022 | 1 | 0 | 1 |
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Below are the most recent publications written about "Hypoparathyroidism" by people in Profiles.
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Maksimoski M, Bauer AJ, Kazahaya K, Manning SC, Parikh SR, Simons JP, D'Souza J, Maddalozzo J, Purkey MR, Rychlik K, Ho B, Rutter MJ, Jiang W, Prager JD, Diercks G, Propst EJ, Miyamoto RC, Stack BC, Randolph GW, Rastatter JC. Outcomes in Pediatric Thyroidectomy: Results From a Multinational, Multi-institutional Database. Otolaryngol Head Neck Surg. 2022 11; 167(5):869-876.
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Akturk HK, Yasa S. Previously unreported abnormalities in Wolfram Syndrome Type 2. Pediatr Endocrinol Diabetes Metab. 2017; 23(2):107-110.
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Gupta Y, Bhadada SK, Shah VN, Upreti V, Bhansali A, Jain S, Khurana D, Kalara N. Carotid intima media thickness in patients with sporadic idiopathic hypoparathyroidism: a pilot study. Endocr J. 2012; 59(7):555-9.
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Cuneo BF. 22q11.2 deletion syndrome: DiGeorge, velocardiofacial, and conotruncal anomaly face syndromes. Curr Opin Pediatr. 2001 Oct; 13(5):465-72.
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Klein GL, Nicolai M, Langman CB, Cuneo BF, Sailer DE, Herndon DN. Dysregulation of calcium homeostasis after severe burn injury in children: possible role of magnesium depletion. J Pediatr. 1997 Aug; 131(2):246-51.
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Cuneo BF, Driscoll DA, Gidding SS, Langman CB. Evolution of latent hypoparathyroidism in familial 22q11 deletion syndrome. Am J Med Genet. 1997 Mar 03; 69(1):50-5.
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Goepferd SJ, Flaitz CM. Enamel hypoplasia associated with congenital hypoparathyroidism. Pediatr Dent. 1981 Jun; 3(2):196-200.
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Wells SA, Stirman JA, Bolman RM. Parathyroid transplantation. World J Surg. 1977 Nov; 1(6):747-56.
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CERIMELE E, TECCE T. [Observations on a clinical case of primary hypoparathyroidism]. Rass Neurol Veg. 1962 Feb 28; 16:162-7.
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