Marfanoid habitus - intellectual deficit, autosomal recessive (Q94198): Difference between revisions

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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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    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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