Laron syndrome with immunodeficiency (Q88878): Difference between revisions
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Revision as of 15:16, 15 August 2026
Laron syndrome with immunodeficiency is characterised by severe post-natal growth retardation, delayed bone age and facial dysmorphism (prominent forehead, hypoplastic nasal bridge), and low serum IGF-1 concentrations with normal or high GH concentrations, associated with immunodeficiency characterised by moderate lymphopenia which leads to recurrent infections of the skin and respiratory tract.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_142511578 |
||
| English | Laron syndrome with immunodeficiency |
Laron syndrome with immunodeficiency is characterised by severe post-natal growth retardation, delayed bone age and facial dysmorphism (prominent forehead, hypoplastic nasal bridge), and low serum IGF-1 concentrations with normal or high GH concentrations, associated with immunodeficiency characterised by moderate lymphopenia which leads to recurrent infections of the skin and respiratory tract. |
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CID11:ID_142511578
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dki-india-ID_142511578
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