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Differential Diagnosis For Slow Motor Development


List of current finding(s):

Trauma Causes
Birth canal injury, newborn
Surgical, Procedure Complication
Cerebral CSF shunt failure
Infectious Disorders (Specific Agent)
Post encephalitis status
Infected organ, Abscesses
Neoplastic Disorders
Brain tumor
Metabolic, Storage Disorders
Hurler's mucopolysaccharidosis syndrome
Tay-Sachs disease
Combined carboxylase/Biotinidase deficiency
Molybdenum cofactor deficency
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
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
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
Walker-Warburg syndrome (9q34.1)
Hereditary, Familial, Genetic Disorders
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/secondary to illness
Autism/Autistic child
Functional, Physiologic Variant Disorders
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
Fine motor delay
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External Links Related to Slow Motor Development
PubMed (National Library of Medicine)
NGC (National Guideline Clearinghouse)
Medscape (eMedicine)
Harrison's Online (accessmedicine)
NEJM (The New England Journal of Medicine)