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Keutel syndrome
rareKeutel syndrome is characterized by diffuse cartilage calcification, brachytelephalangism, peripheral pulmonary artery stenoses and facial dysmorphism.
- Identifiers
- MONDO:0009495 OMIM:245150Orphanet:85202
- Causal genes
- MGP
- Part of
- Chondrodysplasia punctataCongenital limb malformationMultiple congenital anomalies/dysmorphic syndrome-intellectual disability
- Also known as
- KTLS · pulmonic stenosis brachytelephalangism and calcification of cartilages · pulmonic stenosis-brachytelephalangism-calcification of cartilages syndrome
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