Keutel syndrome
Keutel syndrome is characterised by diffuse cartilage calcification, brachytelephalangism, peripheral pulmonary artery stenoses and facial dysmorphism
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Keutel syndrome
Summary
Keutel syndrome is a developmental defect during embryogenesis[1]. It draws 96 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #127 of 308).[2]
Key Facts
- Keutel syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Keutel syndrome's instance of is recorded as rare disease[4].
- Keutel syndrome's instance of is recorded as class of disease[5].
- Keutel syndrome is a type of multiple congenital anomalies/dysmorphic syndrome-intellectual disability[6].
- Keutel syndrome is a type of genetic syndromic intellectual disability[7].
- Keutel syndrome is a type of syndrome with brachydactyly[8].
- Keutel syndrome's genetic association is recorded as MGP[9].
- Keutel syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_85202[10].
Why It Matters
Keutel syndrome draws 96 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #127 of 308).[2] It has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[11] It is known by 14 alternative names across languages and contexts.[12]