Differential (Click to cross reference) acromicria amniocentesis Angelman syndrome ataxia attention deficit disorder with hyperactivity autism behavior, combative behavioral disorder CAG repeats chromosome 15 comorbidities corpus callosum, lesion of cry, abnormal cry, weak developmental retardation drooling dysmorphic eating disorder electroencephalogram, abnormalities of facial appearance, abnormal failure to thrive familial feeding disorder Fragile-X associated tremor/ataxia-syndrome fragile-X syndrome fragile-X syndrome, carrier gait disorder gene gene mutation genetic counselling genetic diagnosis, prenatal genetic neurologic disorders genetic screening genetic testing growth hormone deficiency hand flapping hyperactivity hyperphagia hypogonadism hypopigmentation of skin hypotonia hypotonia, infants imbalance infertility intellectual deficit intelligence quotient joint hypermobility mental retardation middle cerebellar peduncle, lesion middle cerebellar peduncle, lesion, bilateral misdiagnosis molecular genetics MRI, abnormal neurologic disease, diagnoses of obesity ovarian insufficiency Prader-Labhart-Willi syndrome prenatal diagnosis by amniocentesis review article seizure short stature speech, delayed development of splenium of corpus callosum strabismus suck, poor tantrum temper tantrums testicular enlargement tongue, protrusion of treatment of neurologic disorder tremor tremulousness wide based gait x-linked intellectual deficit x-linked mental retardation

Showing articles 0 to 2 of 2 The Spectrum of Fragile X Disorders NEJM 393:281-288, Hagerman,R.H. & Hagerman,P.J., 2025 Prader-Willi and Angelman Syndromes Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998 Showing articles 0 to 2 of 2