Brachioskeletogenital syndrome
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(Elsahy-Waters syndrome)
Very rare. Dysmorphic syndrome described in three boys from one family, and characterised by mental retardation, hypertelorism, a broad nasal bridge, maxillary hypoplasia, mandibular prognathism, bifid uvula or partial cleft palate, multiple dental cysts, nodules of Schmorl, fused cervical spinal processes, pectus excavatum and penoscrotal hypospadias
Anesthetic implications:
risk of difficult intubation
References :
Updated: February 2018