Differential (Click to cross reference) CAT scan, abnormal cerebral cortical atrophy children chromosomal abnormality Clinical Pathologic Conference(C.P.C.) contractures, joint creatine phosphokinase(CPK)elevated cry, weak developmental disability developmental milestones developmental retardation disability, neurological dystrophin electromyogram feeding disorder fetal movements, reduced fetus floppy infant gene mutation histochemistry histochemistry of muscle hydrocephalus hypotonia hypotonia, infants leukodystrophy mental retardation merosin MRI MRI, abnormal muscle biopsy muscle weakness muscular dystrophy muscular dystrophy, central nervous system abnormality muscular dystrophy, congenital muscular dystrophy, congenital, Fukuyama type neurologic disease, diagnoses of polymicrogyria polymyositis polymyositis, infantile prognosis respiratory failure review article skin, biopsy suck, poor term infant walking, difficulty with weakness, congenital weakness, generalized white matter disease

Showing articles 0 to 6 of 6 Case 35-2006: A Newborn Boy with Hypotonia NEJM 355:2132-2142, Brown,R.H.,et al, 2006 Congenital Muscular Dystrophy:Use of Brain MR Imaging to Predict Merosin Deficiency Radiology 206:811-816, Lamer,S.,et al, 1998 Diagnosis of Merosin (Laminin-2) Deficient Congenital Muscular Dystrophy by Skin Biopsy Lancet 347:582-584, Sewry,C.A.,et al, 1996 Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form Neurol 46:815-818, Kobayashi,O.,et al, 1996 Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining Neurol 46:810-814, Connolly,A.M.,et al, 1996 Congenital Muscular Dystrophy with Primary Laminin a2 (Merosin) Deficiency Presenting as Inflammatory Myopathy Ann Neurol 40:782-791, Pegoraro,E.,et al, 1996 Showing articles 0 to 6 of 6