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Differential Diagnosis For Slow Motor Development

List of current finding(s):

Slow Motor Development
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Trauma Causes: Birth canal injury, newborn
Surgical, Procedure Complication: Cerebral CSF shunt failure
Infectious Disorders (Specific Agent): Post encephalitis status
Infected organ, Abscesses: Encephalopathy/secondary/toxic/sepsis
Neoplastic Disorders: Brain tumor
Metabolic, Storage Disorders: Hurler's mucopolysaccharidosis syndrome; Tay-Sachs disease; Combined carboxylase/Biotinidase deficiency; Molybdenum cofactor deficency; Phenylketonuria/PKU; Propionicacidemia/ketotic glycinemia; Acyl-CoA Dehydrogenase/short chain def; Cerebral lipidosis disorder; LCHAD/Long chain OH-CoA dehydrogenase def; MCAD/Medium chain OH-CoA Dehydrogenase def; Ornithine Transcarbamylase (OTC) defic.; Succinic Semialdehyde dehydrogenase Deficiency; Tyrosinemia, hereditary; VLCHAD/Very Long chain OH-CoA dehydrogenase def; Alpha-NAGA deficency (Schindler); Fucosidosis (Anderson-Fabry); Gaucher's disease; Homocystinuria/homocystinemia; Hurler-Scheie compound syndrome/mucopol; Niemann-Pick disease; Sanfilippo's mucopolysaccharidosis synd; Tetrahydrobiopterin deficiency/Atypical PKU; Urea cycle/metabolic disorder; Barth Syndrome/3 MethylGlutoconic aciduria/MGA II
Deficiency Disorders: Malnutrition, fetal; Malnutrition, secondary; Malnutrition/Starvation
Congenital, Developmental Disorders: Cerebral palsy; Deafness, congenital; Down's Syndrome; Mental retardation; Asperger syndrome (mild autism); CHARGE Congenital syndrome; Hydrocephalus, obstructive; Congenital cyanotic heart disease; Congenital heart disease; Congenital syndromes; Hydrocephalus, communicating; Dandy-Walker anomaly/syndrome; Happy puppet syndrome/Angelman syndrome; Cerebral gigantism of childhood (Sotos); King Syndrome; Prader-Willi syndrome; Robinow dwarfing syndrome/mesomelic dys; Septo-optic Dysplasia (DeMorsier); Silver-Russell syndrome; Singleton-Merten syndrome; Velocardiofacial (22q gene) syndrome; Curry-Jones Syndrome; Hydrocephalus; Walker-Warburg syndrome (9q34.1)
Hereditary, Familial, Genetic Disorders: Ataxia-telangiectasia; Infantile neuroaxonal dystrophy; Chromosome 22q13.3 deletion syndrome (22q13.3); Juberg Marsidi Genetic syndrome (unco); Timothy Calcium channel anomaly; MELAS Encephalopathy; Dominant SCA/Spinal Cerebellar ataxias; Cerebellar ataxia, congenital/hered.; Dysautonomia, familial; Dystonia musculorum deformans; Hereditary mitochondrial disorder; SHORT syndrome (Rieger anomaly plus); Torsion dystonia, primary/idiopathic; Chromosome 20 deletion/Ring syndrome; Faciocardiorenal Syndrome (Eastman-Bixler); Segawa Syndrome/Infant Parkinsonism
Relational, Mental, Psychiatric Disorders: Depression; Depression/secondary to illness; Autism/Autistic child
Functional, Physiologic Variant Disorders: Abuse/neglect; Chronic illness; Sensory deprivation/status
Vegetative, Autonomic, Endocrine Disorders: Epilepsy, petit mal, myoclonic, astatic; Hydrocephalus Syndrome
Poisoning (Specific Agent): Lead poisoning in children; Lead poisoning; Fetal alcohol syndrome; Lead encephalopathy; Mercury poisoning/infant/child
Synonyms: Fine motor delay
Definition: Be the first to add a definition for Slow Motor Development
External Links Related to Slow Motor Development: Google; Wikipedia; Merck; Images; PubMed (National Library of Medicine); NGC (National Guideline Clearinghouse); Medscape (eMedicine); Harrison's Online (accessmedicine); NEJM (The New England Journal of Medicine)

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