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Differential Diagnosis For Head Lag Infant Sign
- Infected organ, Abscesses
Newborn Sepsis Syndrome- Allergic, Collagen, Auto-Immune Disorders
Dermatomyositis
Dermatomyositis/childhood type- Metabolic, Storage Disorders
Kernicterus
Tay-Sachs disease
Methylmalonic acidemia/ketotic glycine
Glycogen storage muscle disease/Pompe- Deficiency Disorders
Rickets (vitamin D deficiency)- Congenital, Developmental Disorders
Down's Syndrome
Cretinism
Allan-Herndon Mental Retardation/X-linked
Aicardi syndrome
Achondroplasia
Amyotonia, congenita
Corpus callosum agenesis
Hypotonia of Werdnig-Hoffman
Prader-Willi syndrome
Trisomy 13 syndrome
Central Hypotonia Infants- Hereditary, Familial, Genetic Disorders
Duchenne's Muscular Dystrophy/Pseudohypertrophic
Marfan's syndrome
Muscular dystrophy
Muscular dystrophy, progressive
Canavan disease
Cerebellar ataxia, congenital/hered.
Dysautonomia, familial
Facioscapulohumeral muscular dystrophy
Leukodystrophy, Krabbe
Muscular atrophy, infantile, spinal
Oculopharyngeal muscular dystrophy- Usage, Degenerative, Necrosis, Age Related Disorders
Amyotrophic lateral sclerosis
Progressive bulbar palsy (Duchenne)
Metachromatic leukodystrophy- Anatomic, Foreign Body, Structural Disorders
Spondylosis, cervical
Cervical spinal stenosis- Functional, Physiologic Variant Disorders
Bed rest, prolonged- Vegetative, Autonomic, Endocrine Disorders
Myasthenic crisis
Myasthenia gravis
Myasthenic syndrome (Pseudomyasthenia)- Reference to Organ System
Ataxia, cerebellar, acute
Cerebellar syndrome, acquired- Drugs
Hypervitaminosis D- Poisoning (Specific Agent)
Botulism
Botulism, infant- Definition
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- External Links Related to Head Lag Infant Sign
- 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)