Pseudohypoparathyroidism history and symptoms: Difference between revisions
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===Symptoms=== | ===Symptoms=== | ||
*The most common symptoms of pseudohypoparathyroidism type 1a include [[short stature]],[[mental retardation]] associated with [[Albright's hereditary osteodystrophy|Albright hereditary osteodystrophy]] [[phenotype]]. | *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]]. | ||
*Common symptoms due to associated [[hypocalcemia]] include | *Common symptoms due to associated [[hypocalcemia]] include | ||
Revision as of 14:56, 2 October 2017
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Differentiating Pseudohypoparathyroidism from other Diseases |
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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
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.
- Common symptoms due to associated hypocalcemia include
- Paresthesias (peri-oral, extremities)
- Muscle twitching
- Carpopedal spasm
- Seizures
- Prolonged QT interval
- Hypotension
- Arrhythmia