Differential (Click to cross reference) acromicria amniocentesis Angelman syndrome ataxia behavior, combative behavioral disorder chromosomal abnormality chromosome 15 cold hands sign corpus callosum, atrophy of corpus callosum, thinning cry, abnormal cry, weak developmental milestones, loss of developmental retardation diagnostic criteria drooling dysmorphic eating disorder electroencephalogram, abnormalities of encephalopathy facial appearance, abnormal failure to thrive feeding disorder finger tapping gait disorder gender gene gene mutation genetic counselling genetic diagnosis, prenatal genetic neurologic disorders genetic testing genital hypoplasia growth hormone deficiency growth retardation hand flapping hyperphagia hypogonadism hypopigmentation of skin hypotonia hypotonia, infants imbalance intellectual deficit intellectual deterioration mental retardation microcephaly misdiagnosis molecular genetics MRI, abnormal neurologic disease, diagnoses of obesity postural abnormality Prader-Labhart-Willi syndrome prenatal diagnosis by amniocentesis Rett's syndrome review article scoliosis scoliosis, neurologic association with seizure short stature spasticity stereotyped behavior strabismus suck, poor temper tantrums tongue, protrusion of tremulousness wheelchair wide based gait

Showing articles 0 to 3 of 3 A Middle-aged Woman with Severe Scoliosis and Encephalopathy JAMA Neurol 78:251-252, Mohan, G.,et al, 2021 Prader-Willi and Angelman Syndromes Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998 Physical Features of Prader-Willi Syndrome in Neonates Am J Dis Child 144:1251-1254, Aughton,D.J.&Cassidy,S.B., 1990 Showing articles 0 to 3 of 3