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- W1519057207 abstract "Smith-Magenis syndrome (SMS) is characterized by distinctive facial features that progress with age, developmental delay, cognitive impairment, and behavioral abnormalities associated with molecular anomaly in 17p11.2. Treatment includes: early childhood intervention programs, special education, vocational training later in life, and speech/language, physical, and occupational, behavioral, and sensory integration therapies. We report a 14-year-old girl with mental retardation, behavioral abnormalities and facial dysmorphism, with SMS diagnosis confirmed by cytogenetic analysis and in situ hydridization (FISH)." @default.
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- W1519057207 date "2008-04-01" @default.
- W1519057207 modified "2023-09-26" @default.
- W1519057207 title "[Smith-Magenis syndrome: case report and review]." @default.
- W1519057207 doi "https://doi.org/10.1590/s0325-00752008000200009" @default.
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