Disease Information for Muscular atrophy, infantile, spinal

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Clinical Manifestations
Signs & Symptoms
Hyperextensable Joints Infant
Tongue Protrudes Infant
Central hypotonia, infants
Delay Sitting Unsupported Infant
Head Lag Infant Sign
Hypotonia
Mouth Hangs Open Infant
Muscle Atrophy
Muscle weakness
Muscles Soft/Doughy Infant
Neck weakness/head nodding
Rolling Over Delay Infant
Weak/Weak as a kitten (symptom)
Babkin infant sign/Abnormal
Delayed walking milestone/child
Development Motor Skills (Milestones) Delayed
Galant Infant reflex/Abnormal
Head Neck Floppy Infant Hypotonia Sign
Infant Head Support Delay
Moro reflex Poor/Absent Infant
Palmar Grasp infant Reflex Abnormal
Primitive infant reflexes/Abnormal
Rooting infant sign/Abnormal
Swimming infant reflex/Abnormal
Tonic Neck Infant reflex/Abnormal
Weakness/Diffuse motor loss
Shallow Breathing Infant
Enervated/extreme acute fatigue
Muscle Wasting/Diffuse
Weakness
Clinical Presentation & Variations
Early Childhood/Infancy Muscular Dystrophy
Disease Progression
Course/Chronic disorder
Course/Chronic only
Demographics & Risk Factors
Population Group
Child
Infant
Population/Pediatrics population
Family History
Family history/Parental consanguinity
Sex & Age Groups
Population/Child
Population/Child-Infant Only
Population/Children/all
Population/Infant
Laboratory Tests
Abnormal Lab Findings - Increased
Aldolase, serum (Lab)
Diagnostic Test Results
Pathology
BX/Muscle Biopsy Abnormal
Electrodiagnosis
EMG/Abnormal findings
Associated Diseases & Rule outs
Associated Disease & Complications
Motor neuron disease
Neonatal Hypotonia/Floppy Baby Syndrome
Paraplegia
Disease Mechanism & Classification
Class
CLASS/Pediatric disorders (ex)
CLASS/Motor neuron/unit disorder (ex)
CLASS/Muscle disorder (ex)
CLASS/Muscle/tendon/extremities (category)
Pathophysiology
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Process
PROCESS/Atrophic disorders (ex)
PROCESS/Autosomal recessive disorder (ex)
PROCESS/Hereditofamilial (category)
PROCESS/Use/Age/atrophic disorder (category)
Synonyms
Synonym
atrophy muscle spinal infantile type I (Werdnig Hoffmann), Disease Werdnig Hoffman, Disease Werdnig Hoffmann, Diseases Werdnig Hoffman, HMN (Hereditary Motor Neuropathy) Proximal Type I, HMN Proximal Type I, Hoffman Disease Werdnig, Hoffman Diseases Werdnig, Infant spinal muscular atrophy, infantile muscular atrophy, Infantile spinal muscular atrophy, Infantile spinal muscular atrophy type I (Werdnig Hoffman), muscle atrophy spinal infantile type I (Werdnig Hoffmann), MUSCULAR ATROPHY INFANTILE, Muscular Atrophy Spinal Infantile, Muscular Atrophy Spinal Type I, Progressive muscular atrophy of infancy, Proximal Hereditary Motor Neuropathy Type I, SMA I, SMA INFANTILE ACUTE FORM, SMA1, Spinal muscular atrophy infantile, Spinal muscular atrophy type I, Type I Spinal Muscular Atrophy, Werdnig Hoffman Disease, Werdnig Hoffman Diseases, Werdnig Hoffmann, WERDNIG HOFFMANN DIS, Werdnig Hoffmann Disease, Werdnig Hoffmann disease (disorder), WHD Werdnig Hoffmann disease, Synonym/Werdnig-Hoffmann paralysis
Definition
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External Links Related to Muscular atrophy, infantile, spinal
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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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