Keutel syndrome is a rare autosomal recessive disorder characterized by diffuse cartilage calcification, characteristic physiognomy, brachytelephalangism, peripheral pulmonary stenosis, hearing loss, and borderline to mild mental retardation. We report on an Arab boy with Keutel syndrome and cerebra
Keutel syndrome: Clinical report and literature review
โ Scribed by Cormode, Edward J. ;Dawson, Malcolm ;Lowry, R. Brian ;Opitz, John M. ;Reynolds, James F.
- Publisher
- John Wiley and Sons
- Year
- 1986
- Tongue
- English
- Weight
- 397 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0148-7299
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