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Learn more 1p36 deletion syndrome (monosomy 1p36 syndrome) is characterized by a deletion on the short arm of chromosome 1.

The disorder is characterized by dysmorphic craniofacial features, developmental delay, brain abnormalities, short feet, severe congenital heart defects, hypotonia, and brachy-/camptodactyly. Learn more Both Angelman (AS), a maternal deletion, and Prader-Willi (PWS), a paternal deletion, syndromes are caused by deletions on the long arm of chromosome 15. The American College of Obstetricians and Gynecologists Committee on Genetics and the Society for Maternal-Fetal Medicine Publications Committee.

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