Pseudohypoparathyroidism history and symptoms: Difference between revisions
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==Overview== | ==Overview== | ||
A positive family history of pseudohypoparathyroidism is suggestive of the [[autosomal dominant]] inheritance.The most common symptoms of pseudohypoparathyroidism type 1a include [[short stature]],short limbs,[[mental retardation]] associated with [[Albright's hereditary osteodystrophy|Albright hereditary osteodystrophy]] [[phenotype]]. | |||
==History and Symptoms== | ==History and Symptoms== | ||
Revision as of 16:34, 2 October 2017
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Mazia Fatima, MBBS [2]
Overview
A positive family history of pseudohypoparathyroidism is suggestive of the autosomal dominant inheritance.The most common symptoms of pseudohypoparathyroidism type 1a include short stature,short limbs,mental retardation associated with Albright hereditary osteodystrophy phenotype.
History and Symptoms
History
- A positive family history of pseudohypoparathyroidism is suggestive of the autosomal dominant inheritance.
Symptoms
- The most common symptoms of pseudohypoparathyroidism type 1a include short stature,short limbs,mental retardation associated with Albright hereditary osteodystrophy phenotype.[1]
- Common symptoms due to associated hypocalcemia include
- Paresthesias (peri-oral, extremities)
- Muscle twitching
- Carpopedal spasm
- Seizures
- Prolonged QT interval
- Hypotension
- Arrhythmia
References
- ↑ Mantovani G, Elli FM, Corbetta S (2017). "Hypothyroidism associated with parathyroid disorders". Best Pract. Res. Clin. Endocrinol. Metab. 31 (2): 161–173. doi:10.1016/j.beem.2017.04.004. PMID 28648505.