Smith–Magenis syndrome
Human disease
Smith–Magenis syndrome
Smith–Magenis syndrome (SMS), also known as 17p-microdeletion syndrome, is a microdeletion syndrome characterized by an abnormality in the short (p) arm of chromosome 17. It has features including intellectual disability, facial abnormalities, difficulty sleeping, and numerous behavioral problems such as self-harm. Smith–Magenis syndrome affects an estimated between 1 in 15,000 to 1 in 25,000 individuals.
Read on Wikipedia · Image Sironi, A., Bestetti, I., Masciadri, M. et al., CC BY 4.0
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