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Keutel syndrome  

Definición

  • Keutel syndrome (KS) is a rare autosomal recessive genetic disorder characterized by abnormal diffuse cartilage calcification, hypoplasia of the mid-face, peripheral pulmonary stenosis, hearing loss, short distal phalanges (tips) of the fingers and mild mental retardation. (Wikipedia)

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URI

http://data.loterre.fr/ark:/67375/VH8-KN1MVJP1-7

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