Title: Prader-Willi Association (USA)
Description: Prader-Willi Syndrome
Keywords:Prader-Willi Syndrome, PWSAUSA, Prader-Willi Syndrome Association, PWS, genetics, prader-willi research, prader-willi syndrome research, skin picking, obesity, chromosome 15, Obsessive Compulsive Behavior, developmental delay, failure to thrive, growth hormone, hyperphagia, hypothalamus, muscle weakness, hypotonia, uniparental disomy, UPD, small hands and feet, hypoganadism, hypogenitalism, body composition, obsessive-compulsive behavior,
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self-injurious behavior, rectal picking, eating disorder, food seeking, narrow bi-frontal diameter, short stature, growth hormone therapy, infantile hypotonia, feeding difficulties, poor suck reflex, scoliosis, gastric distension or rupture, ghrelin, peptide YY, neuropeptides, genomic imprinting, 15q11-q13 region, SNRPN, imprinting defects mutations, paternal deletion, maternal disomy, heterodisomy, isodisomy, epimutations, fatness patterns, insulin resistance, decreased muscle mass, energy balance or expenditures, metabolic rate, transgenic mice, SSRIs, relaxation of imprinting, natural history, quality of life, life-threatening obesity, contiguous gene syndrome, microdeletion, hypopigmentation, enamel hypoplasia, diagnostic criteria, sticky saliva, temperature instability, decreased pain sensation, gastrostomy tube, decreased fetal movement, breech delivery, diet control, orexigenic, visual memory, verbal IQ, type 2 diabetes, osteoporosis, DEXA, fat-free mass, microarray gene expression, GABA, BMI, type I and II deletions, genotype/phenotype correlations, inedible food items, sleep disorders, dolichocephaly, strabismus, delayed puberty(View Less)
