Short stature due to growth hormone qualitative anomaly (Q106510): Difference between revisions
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16 August 2026
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Latest revision as of 13:29, 17 August 2026
This syndrome is characterised by growth retardation and short stature (despite the presence of normal or slightly elevated levels of immunoreactive growth hormone, GH), low concentrations of insulin-like growth factor-I (IGF-I) and a significant increase in growth rate following recombinant GH therapy. Prevalence is unknown but only a few cases have been reported in the literature. The syndrome is caused by various mutations in the GH1 gene (17q22-q24) that result in structural GH anomalies and a biologically inactive molecule. Transmission is autosomal recessive.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1665498704 |
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| English | Short stature due to growth hormone qualitative anomaly |
This syndrome is characterised by growth retardation and short stature (despite the presence of normal or slightly elevated levels of immunoreactive growth hormone, GH), low concentrations of insulin-like growth factor-I (IGF-I) and a significant increase in growth rate following recombinant GH therapy. Prevalence is unknown but only a few cases have been reported in the literature. The syndrome is caused by various mutations in the GH1 gene (17q22-q24) that result in structural GH anomalies and a biologically inactive molecule. Transmission is autosomal recessive. |
Statements
CID11:ID_1665498704
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dki-india-ID_1665498704
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Concluído
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16 August 2026
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