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Differential Diagnosis For Psychomotor retardation
- Neoplastic Disorders
Craniopharyngioma- Metabolic, Storage Disorders
Mucopolysaccharidoses
Hurler's mucopolysaccharidosis syndrome
Tay-Sachs disease
Hydroxyprolinemia, congenital
Combined carboxylase/Biotinidase deficiency
Ketotic hyperglycinemia, idiopathic
Methylmalonic acidemia/ketotic glycine
Phenylketonuria/PKU
Propionicacidemia/ketotic glycinemia
Pyruvate Dehydrogenase Complex Deficiency/PDCD
Adenyl succinate lysate deficiency
Cerebral Gaucher's of infants (acute)
Cerebral lipidosis disorder
Hyperglycinemia, nonketotic
Lysinemia
Prolinemia/type II
Saccharopinuria/lysine metabolism defect
Sialidosis/Cherry Red Spot Myoclonus
Alpha-NAGA deficency (Schindler)
Aminoaciduria
Aspartylglycosaminuria
DiFerrente syndrome (Mucopolysaccharidosis VIII)
Fucosidosis (Anderson-Fabry)
Gangliosidosis, generalized (GM1)
Glutaric aciduria/Acidemia
Infantile ceroid lipofuscinosis/Finnish (Santvuori-Haltia)
Juvenile ceroid lipofuscinosis/Batten-M
Lesch-Nyhan syndrome
Mannosidosis
Maple syrup urine disease
Morquio's mucopolysaccharidosis synd.
Mucolipidosis IV (Bermans Syndrome)
Niemann-Pick disease
Pipecolic acidemia
Sanfilippo's mucopolysaccharidosis synd
Tetrahydrobiopterin deficiency/Atypical PKU
Urea cycle/metabolic disorder- Congenital, Developmental Disorders
Cerebral palsy
CHARGE Congenital syndrome
Allan-Herndon Mental Retardation/X-linked
Joubert syndrome/absent cerebellar vermis (unco)
Kenny-Caffey syndrome/KCS (1q42-q43)
Alexander disease
Happy puppet syndrome/Angelman syndrome
Cerebral gigantism of childhood (Sotos)
De Lange syndrome
Rett's syndrome
Roaf's syndrome
Septo-optic Dysplasia (DeMorsier)
Smith Magenis syndrome
Sturge-Weber disease
Velocardiofacial (22q gene) syndrome
XYY Syndrome
CODAS Syndrome
Landau-Kleffner Syndrome
Porteous Syndrome
Ruvacaba's Syndrome
Weaver syndrome (Marshall-Smith)- Hereditary, Familial, Genetic Disorders
Ataxia-telangiectasia
Infantile neuroaxonal dystrophy
Neurofibromatosis
Tuberous Sclerosis
Johanson Blizzard genetic syndrome (unco)
Schilder disease/Adrenoleukodystrophy
MELAS Encephalopathy
Canavan disease
Cockayne syndrome
Facial ectodermal dysplasia (Setleis)
Hereditary mitochondrial disorder
Hermann's syndrome
Menkes steely hair disease
Pelizaeus-Merzbacher disease
Von Hipple-Lindau disease/Retinocerebellar angiomas
Cerebellar ataxia/Cayman type
Cowden disease/CD (10q23.31)
Neuhauser Syndrome- Usage, Degenerative, Necrosis, Age Related Disorders
Binswanger's dementia
Metachromatic leukodystrophy- Relational, Mental, Psychiatric Disorders
Suicide/Suicidal depression
Depression
Depression, endogenous
Depression, reactive
Autism/Autistic child- Vegetative, Autonomic, Endocrine Disorders
Seizures
Hypothyroidism (myxedema)
Apathetic thyroid crisis- Reference to Organ System
Osteopathia striata with cranial stenosis- Synonyms
- Motor retardation, Motor retardation (finding), Slow to move
- Definition
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- External Links Related to Psychomotor retardation
- 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)