Differential (Click to cross reference) acromicria advances in neurology amniocentesis Angelman syndrome areflexia ataxia autism behavior, combative behavioral disorder children chromosomal abnormality chromosome 15 cry, abnormal cry, weak cryptorchidism developmental retardation drooling dysmorphic ear, abnormal eating disorder electroencephalogram, abnormalities of facial appearance, abnormal failure to thrive feeding disorder fetal alcohol syndrome fragile-X syndrome gait disorder gene genetic counselling genetic diagnosis, prenatal genetic neurologic disorders genital hypoplasia growth hormone deficiency hand flapping high arched palate hyperphagia hypertelorism hypogonadism hypopigmentation of skin hypotonia hypotonia, infants imbalance intelligence quotient learning disability learning disability, in children mental retardation micrognathia misdiagnosis molecular genetics mongolism mortality neurologic disease, diagnoses of obesity Prader-Labhart-Willi syndrome precocious puberty prenatal diagnosis by amniocentesis prognosis psychiatric disorder psychological testing psychological testing, children review article seizure short stature strabismus suck, poor temper tantrums tongue, protrusion of treatment of neurologic disorder tremulousness wide based gait

Showing articles 0 to 5 of 5 Learning Disability Lancet 362:811-821, Gillberg,C.&Soderstrom,H., 2003 Prader-Willi and Angelman Syndromes Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998 Diagnostic Test for the Prader-Willi Syndrome by SNRPN Expression in Blood Lancet 348:1068-1069, Wevrick,R.&Francke,U., 1996 Physical Features of Prader-Willi Syndrome in Neonates Am J Dis Child 144:1251-1254, Aughton,D.J.&Cassidy,S.B., 1990 Prader-Willi-Syndrome, In Endocrine & Genetic Diseases of Childhood & Adolescence (Ed) , 1975. W. B. Saunders Co, p, Gardner,L.I., 1975 Showing articles 0 to 5 of 5