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Differential Diagnosis For Head Lag Infant Sign

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List of current finding(s):

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
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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