Laron syndrome (Q669822)
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congenital disorder characterized by marked short stature associated with normal or high serum growth hormone (GH) and low serum insulin-like growth factor-1 (IGF-I) levels which fail to rise after exogenous GH administration
- Laron-type isolated somatotropin defect (disorder)
- Laron-type isolated somatotropin defect
- Growth Hormone Receptor Deficiency
- Primary growth hormone resistance
- Laron-type dwarfism
- Pituitary Dwarfism 2
- Growth Hormone Insensitivity Syndrome
- Primary GH insensitivity
- Short stature due to growth hormone resistance
- Complete growth hormone insensitivity
- Primary GH resistance
- GH receptor deficiency
- Primary growth hormone insensitivity
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Laron syndrome |
congenital disorder characterized by marked short stature associated with normal or high serum growth hormone (GH) and low serum insulin-like growth factor-1 (IGF-I) levels which fail to rise after exogenous GH administration |
|
Statements
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Identifiers
1 reference
Laron Syndrome
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Sitelinks
Wikipedia(17 entries)
- arwiki متلازمة لارون
- cswiki Laronův syndrom
- dewiki Laron-Syndrom
- enwiki Laron syndrome
- eswiki Síndrome de Laron
- fawiki سندرم لارون
- fiwiki Laronin oireyhtymä
- frwiki Syndrome de Laron
- hewiki תסמונת לרון
- itwiki Sindrome di Laron
- jawiki ラロン症候群
- kowiki 라론 증후군
- plwiki Karłowatość typu Larona
- ruwiki Синдром Ларона
- svwiki Larons syndrom
- trwiki Laron sendromu
- ukwiki Синдром Ларона