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Differential Diagnosis For Development Motor Skills (Milestones) Delayed: Congenital, Developmental Disorders
List of current finding(s):
Development Motor Skills (Milestones) Delayed
- Trauma Causes (5)
- Electromagnetic, Physics, trauma, Radiation Causes (1)
- Surgical, Procedure Complication (1)
- Infectious Disorders (Specific Agent) (12)
- Infected organ, Abscesses (2)
- Neoplastic Disorders (1)
- Metabolic, Storage Disorders (42)
- Biochemical Disorders (1)
- Deficiency Disorders (3)
- Congenital, Developmental Disorders (46)
- Hereditary, Familial, Genetic Disorders (46)
- Usage, Degenerative, Necrosis, Age Related Disorders (2)
- Relational, Mental, Psychiatric Disorders (3)
- Anatomic, Foreign Body, Structural Disorders (1)
- Functional, Physiologic Variant Disorders (4)
- Vegetative, Autonomic, Endocrine Disorders (6)
- Reference to Organ System (2)
- Pathophysiologic (2)
- Drugs (2)
- Poisoning (Specific Agent) (8)
- Organ Poisoning (Intoxication) (1)
- Synonyms (14)
- Definition
- External Links Related to Development Motor Skills (Milestones) Delayed
- Congenital, Developmental Disorders:
- Cerebral palsy
- Fetal CNS disorder
- 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
- Hemiplegia, infantile
- Hydrocephalus, communicating
- Meningomyelocele
- Spina bifida
- Cretinism
- Spastic diplegia cerebral palsy
- Syringomyelia
- Trisomy-21 partial translocation
- Allan-Herndon Mental Retardation/X-linked
- Shprintzen-Goldberg craniosynostosis syndrome (15q21.1)
- Alexander disease
- Dandy-Walker anomaly/syndrome
- Happy puppet syndrome/Angelman syndrome
- Amyotonia, congenita
- Cerebral gigantism of childhood (Sotos)
- Corpus callosum agenesis
- King Syndrome
- Prader-Willi syndrome
- Robinow dwarfing syndrome/mesomelic dys
- Rubinstein-Taybi syndrome
- Septo-optic Dysplasia (DeMorsier)
- Silver-Russell syndrome
- Singleton-Merten syndrome
- Trisomy 13 syndrome
- Trisomy-18 syndrome
- Velocardiofacial (22q gene) syndrome
- Birth asphyxia Syndrome/Hypoxic event
- Central Hypotonia Infants
- Cerebral Dysgenesis
- Coffin-Lowry Syndrome
- Curry-Jones Syndrome
- Fetal CVA disorder
- Hydrocephalus
- Merosin Deficient Muscular Dystrophy
- Walker-Warburg syndrome (9q34.1)
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