| Document Date: 2014-05-30 13:36:37
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Facility Congenital TORCH complex / Syndrome Tay-Sachs Disease TORCH complex / / MedicalCondition Involvement - lumbar Spinal Cord Injury / Retinopathy of Prematurity / Tay-Sachs Disease TORCH / Muscular Dystrophy / II Werdnig-Hoffman Syndrome Williams Syndrome Wolf-Hirschhorn Syndrome / Persistent Pulmonary / Rett Syndrome Reduction Deformities / Moderate Hypoxic Ischemic Encephalopathy / Encephalocele Epilepsy / myoclonic epilepsy / Toxoplasmosis / Congenital Myopathy Congenital Rubella Cornelia de Lange Syndrome Craniostenosis Cri-du-chat Syndrome Di George Syndrome / Impairment - Unspecified Visual Loss Vitreous anomalies Warrdenburg Syndrome / Corpus Callosum Alagille Syndrome / Newborn Hypothyroidism / Down Syndrome Dravet Syndrome / Mild Hypoxic Ischemic Encephalopathy / Hoffman Syndrome Aphakia Argininemia Arthrogryposis Autism / Epilepsy / PKU untreated Phelan McDermid Syndrome / aka Arteriohepatic Dysplasia / Motor Neuron Diseases Mucolipidoses / Hypoxic Ischemic Encephalopathy / Niemann-Pick Disease Noonan Syndrome Optic Atrophy Optic Nerve Hypoplasia Osteogenesis Imperfecta Paraplegia Pervasive Developmental Disorder Peters' Anomaly Phthisis Bulbi Pierre-Robin Deformity / Hunter Syndrome Hurler Syndrome Hydrocephalus Hypertension / Shaken Baby Syndrome Sly Syndrome Soto Syndrome Spina Bifida Spinal Cord Injury / Seizure Disorder / Syndrome / unspecified Hearing Loss / Angelman Syndrome Aniridia Anterior Horn Cell Disorders / Syndrome Maple Syrup Urine Disease Methylmalonic Acidemia Microcephalus Microphthalmos Mitochondrial Disorder Mobius Syndrome / / Person Cornelia de Lange / Cataract Congenital Cytomegalovirus Congenital Glaucoma / Pierre-Robin Deformity / / Position Hunter / / Product Thrive / /
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Diagnosis Agenesis or partial agenesis of the Corpus Callosum Alagille Syndrome (aka Arteriohepatic Dysplasia) Angelman Syndrome Aniridia Anterior Horn Cell Disorders - Werdnig - Hoffman Syndrome