Marfanoid habitus - intellectual deficit, autosomal recessive (Q94198): Difference between revisions
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Latest revision as of 09:19, 16 August 2026
Marfanoid habitus intellectual deficit, autosomal recessive is a very rare multiple congenital anomalies syndrome described in four sibs and characterised by intellectual deficit, flat face and some skeletal features of Marfan syndrome such as tall stature, dolichostenomelia, arm span larger than height, arachnodactyly of hands and feet, little subcutaneous fat, muscle hypotonia and intellectual deficit.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_699821839 |
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| English | Marfanoid habitus - intellectual deficit, autosomal recessive |
Marfanoid habitus intellectual deficit, autosomal recessive is a very rare multiple congenital anomalies syndrome described in four sibs and characterised by intellectual deficit, flat face and some skeletal features of Marfan syndrome such as tall stature, dolichostenomelia, arm span larger than height, arachnodactyly of hands and feet, little subcutaneous fat, muscle hypotonia and intellectual deficit. |
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CID11:ID_699821839
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dki-india-ID_699821839
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Concluído
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15 August 2026
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