Short stature due to growth hormone resistance (Q92538): Difference between revisions
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Síndrome de Laron é um transtorno genético congênito caracterizado por baixa estatura importante associada a níveis séricos normais ou elevados de hormônio do crescimento (GH) e baixos níveis séricos do fator de crescimento semelhante a insulina 1 ( IGF-1) que não aumentam após a administração de GH exógeno. | |||
| description / en | description / en | ||
Laron syndrome is a congenital genetic disorder characterised 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. | |||
Revision as of 07:40, 16 August 2026
Laron syndrome is a congenital genetic disorder characterised 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.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_176353068 |
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| English | Short stature due to growth hormone resistance |
Laron syndrome is a congenital genetic disorder characterised 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. |
