" /> Keutel syndrome - CISMeF





Preferred Label : Keutel syndrome;

ICD-11 definition : Keutel syndrome is an autosomal recessive developmental anomalies syndrome characterised by diffuse cartilage calcification, brachytelephalangism, peripheral pulmonary artery stenoses and facial dysmorphism.;

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Keutel syndrome is an autosomal recessive developmental anomalies syndrome characterised by diffuse cartilage calcification, brachytelephalangism, peripheral pulmonary artery stenoses and facial dysmorphism.

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28/07/2025


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