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Facial dysmorphism-shawl scrotum-joint laxity syndrome
Disease definition
Facial dysmorphism-shawl scrotum-joint laxity syndrome is characterised by facial dysmorphism (hypertelorism, telecanthus, downslanting palpebral fissures, ptosis, malar hypoplasia, broad nasal bridge, thin upper lip, smooth philtrum, and low-set prominent ears) and associated with joint anomalies (genu valgum or cubitus valgus, hyper-extensible joints, etc.). It has been described in two patients (a mother and her son). The boy also had hypoplastic shawl scrotum and cryptorchidism, and the mother had mild intellectual deficit.
ORPHA:1778
Classification level: Disorder- Synonym(s):
- Seaver-Cassidy syndrome
- Prevalence: <1 / 1 000 000
- Inheritance: -
- Age of onset: Neonatal
- ICD-10: Q87.8
- OMIM: -
- UMLS: C2931522
- MeSH: -
- GARD: 4778
- MedDRA: -
A summary on this disease is available in Deutsch (2007) Español (2007) Français (2007) Italiano (2007) Nederlands (2007)
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