Pseudohypoparathyroidism diagnostic criteria: Difference between revisions
Mazia Fatima (talk | contribs) |
Mazia Fatima (talk | contribs) |
||
| Line 13: | Line 13: | ||
**[[Hyperphosphatemia]] | **[[Hyperphosphatemia]] | ||
**Elevated serum concentration of [[parathyroid]] hormone | **Elevated serum concentration of [[parathyroid]] hormone | ||
**Diminished urinary [[cAMP]] response after administration of the biosynthetic N-terminal fragment of [[parathyroid]] hormone | **Diminished urinary [[cAMP]] response after administration of the biosynthetic N-terminal fragment of [[parathyroid]] hormone | ||
*Genetic diagnosis of GNAS mutation is a most definitive method of diagnosis | |||
==References== | ==References== | ||
Revision as of 21:05, 16 October 2017
|
Pseudohypoparathyroidism Microchapters |
|
Differentiating Pseudohypoparathyroidism from other Diseases |
|---|
|
Diagnosis |
|
Treatment |
|
Case Studies |
|
Pseudohypoparathyroidism diagnostic criteria On the Web |
|
American Roentgen Ray Society Images of Pseudohypoparathyroidism diagnostic criteria |
|
Risk calculators and risk factors for Pseudohypoparathyroidism diagnostic criteria |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
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.
Diagnostic Criteria
The diagnosis of pseudohypoparathyroidism type 1a patients includes: [1]
- 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
- Genetic diagnosis of GNAS mutation is a most definitive method of diagnosis
References
- ↑ Tafaj O, Jüppner H (2017). "Pseudohypoparathyroidism: one gene, several syndromes". J. Endocrinol. Invest. 40 (4): 347–356. doi:10.1007/s40618-016-0588-4. PMID 27995443.