Prader-Willi Syndrome Causes, Signs, Symptoms, Diagnosis, and Treatment Information o 

Read about Prader-Willi syndrome, a genetic condition characterized by weak muscle tone, feeding problems, delayed growth and development, which eventually leads to severe obesity. Prader-Willi syndrome is a defect in chromosome 15. Prader-Willi syndrome, severe floppiness (hypotonia), poor growth, delayed development, poor feeding problems in early infancy, excessive eating, fetal development, genetic, genes, inherited, severe obesity, contiguous gene syndrome, hypogonadism, learning disability , mental retardation ; mutation ; overeating, sign, signs, symptom, symptoms, cause, causes, diagnose, diagnosis, treat, treated, treatment, prader willi