Keutel syndrome

English

Etymology

Identified by J. Keutel et al in 1972.

Noun

Keutel syndrome (uncountable)

  1. A rare genetic disorder characterized by abnormal diffuse cartilage calcification, hypoplasia of the mid-face, peripheral pulmonary stenosis, hearing loss, short distal phalanges of the fingers, and mild mental retardation.
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