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Smith-Magenis syndrome is a neurobehavioral and occasionally congenital malformation syndrome with clinical features of mild to moderate cognitive impairment, facial anomalies, atypical behavioral disorders, scoliosis, short stature and characteristic hand and foot anomalies. The condition is usually sporadic with a few familial cases. However, the genetic etiology of Smith-Magenis syndrome has not been clarified, and affected individuals are generally diagnosed postnatally. We describe a 17-month-old girl who was first diagnosed as having developmental delay and central obesity at the age of 11 months. The patient showed facial malformation (a wide brow), atypical behavior (hyposomnia, hand tremor, frequent smiling and atypical vocalization), short stature and congenital hip dislocation. There was no history of seizures, digestive problems, and abnormal movements. Fluorescent in situ hybridization analysis revealed a deletion of the SMC3 gene in 9 of 10 metaphase spreads. This is the first report of Smith-Magenis syndrome associated with a deletion of the SMC3 gene. The patient exhibited atypical facial anomalies and behavioral abnormalities which were compatible with the diagnostic features. Furthermore, a brief family history of congenital hip dislocation suggested autosomal recessive transmission of the mutation.Q:

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