Pseudohypoparathyroidism history and symptoms: Difference between revisions
Jump to navigation
Jump to search
(Created page with "__NOTOC__ {{Pseudohypoparathyroidism}} Please help WikiDoc by adding content here. It's easy! Click here to learn about editing. ==References==...") |
No edit summary |
||
| Line 1: | Line 1: | ||
__NOTOC__ | __NOTOC__ | ||
{{Pseudohypoparathyroidism}} | {{Pseudohypoparathyroidism}} | ||
{{CMG}} | |||
==Overview== | |||
==History and Symptoms== | |||
There are three types of pseudohypoparathyroidism, type 1a, type 1b and type 2. | |||
*Signs and symptoms in type 1b and type 2 | |||
:*[[Numbness]] | |||
:*[[Tetany]] | |||
:*[[Seizures]] | |||
:*[[Cataracts]] | |||
:*Dental problems | |||
*Signs and symptoms in type 1a: Type 1a is inherited in an autosomal dominant manner and is also called Albright's hereditary osteodystrophy. Besides signs in type 1b and type 2, patients with type 1a may have the following symptoms: | |||
:*[[Short stature]]: Round face, short neck, and short hand bones | |||
:*Calcium deposits under the skin | |||
:*Dimples that can replace knuckles on affected fingers | |||
Diseases with similar symptoms | |||
:*[[Hypoparathyroidism (patient information)|Hypoparathyroidism]] | |||
:*[[Rickets (patient information)|Rickets]] | |||
==References== | ==References== | ||
{{Reflist|2}} | {{Reflist|2}} | ||
[[Category:Disease]] | [[Category:Disease]] | ||
Revision as of 14:10, 19 September 2012
|
Pseudohypoparathyroidism Microchapters |
|
Differentiating Pseudohypoparathyroidism from other Diseases |
|---|
|
Diagnosis |
|
Treatment |
|
Case Studies |
|
Pseudohypoparathyroidism history and symptoms On the Web |
|
American Roentgen Ray Society Images of Pseudohypoparathyroidism history and symptoms |
|
Risk calculators and risk factors for Pseudohypoparathyroidism history and symptoms |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
History and Symptoms
There are three types of pseudohypoparathyroidism, type 1a, type 1b and type 2.
- Signs and symptoms in type 1b and type 2
- Signs and symptoms in type 1a: Type 1a is inherited in an autosomal dominant manner and is also called Albright's hereditary osteodystrophy. Besides signs in type 1b and type 2, patients with type 1a may have the following symptoms:
- Short stature: Round face, short neck, and short hand bones
- Calcium deposits under the skin
- Dimples that can replace knuckles on affected fingers
Diseases with similar symptoms