Pseudohypoparathyroidism history and symptoms: Difference between revisions
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==Overview== | ==Overview== | ||
The diagnosis of pseudohypoparathyroidism Type 1a patients includes clinical features of [[Albright's hereditary osteodystrophy]],[[parathyroid]] hormone resistance evidenced by [[hypocalcemia]],[[hyperphosphatemia]],elevated serum concentration of [[parathyroid]] hormone,diminished urinary [[cAMP]] response after administration of the biosynthetic N-terminal fragment of [[parathyroid]] hormone. | The diagnosis of pseudohypoparathyroidism Type 1a patients includes clinical features of [[Albright's hereditary osteodystrophy]],[[parathyroid]] hormone resistance evidenced by [[hypocalcemia]],[[hyperphosphatemia]],elevated serum concentration of [[parathyroid]] hormone,diminished urinary [[cAMP]] response after administration of the biosynthetic N-terminal fragment of [[parathyroid]] hormone. | ||
==History and Symptoms== | |||
===History=== | |||
*A positive family history of pseudohypoparathyroidism is suggestive of the [[autosomal dominant]] inheritance. | *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]],[[mental retardation]] associated with [[Albright's hereditary osteodystrophy|Albright hereditary Osteodystrophy]] [[phenotype]]. | *The most common symptoms of pseudohypoparathyroidism type 1a include [[short stature]],[[mental retardation]] associated with [[Albright's hereditary osteodystrophy|Albright hereditary Osteodystrophy]] [[phenotype]]. | ||
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**[[Hypotension]] | **[[Hypotension]] | ||
**[[Arrhythmia]] | **[[Arrhythmia]] | ||
==References== | ==References== | ||
{{Reflist|2}} | {{Reflist|2}} | ||
Revision as of 13:40, 29 September 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
The diagnosis of pseudohypoparathyroidism Type 1a patients includes clinical features of Albright's hereditary osteodystrophy,parathyroid hormone resistance evidenced by hypocalcemia,hyperphosphatemia,elevated serum concentration of parathyroid hormone,diminished urinary cAMP response after administration of the biosynthetic N-terminal fragment of parathyroid hormone.
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,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