Yes, Prader-Willi syndrome is a noncommunicable disease. It is a genetic disorder caused by the loss of function of specific genes on chromosome 15, typically involving a deletion or an imprinting error. As a noncommunicable condition, it cannot be transmitted from person to person and is instead inherited or occurs spontaneously. The syndrome is characterized by symptoms such as hypotonia, hyperphagia, and developmental delays.
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