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Disease Information for Ataxia Congenital Miosis Syndrome
- Clinical Manifestations
- Signs & Symptoms
- Ataxia
- Spasticity/Spastic gait
- Staggering Gait
- Miosis/narrow pupils
- Demographics & Risk Factors
- Sex & Age Groups
- Population/Child
- Population/Child-Infant Only
- Associated Diseases & Rule outs
- Associated Disease & Complications
- Ataxia Congenital Miosis Syndrome
- Blindness in Children
- Disease Mechanism & Classification
- Class
- CLASS/Neurologic (category)
- CLASS/Eye involvement/disorder (ex)
- Process
- PROCESS/Autosomal dominant hereditary disease (ex).
- PROCESS/Hereditofamilial (category)
- PROCESS/INCIDENCE/Extremely rare disease
- Synonyms
- Synonym
- Synonym/Spastic Ataxia Congenital Miosis
- Definition
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Ataxia spastic congenital miosis: A rare, dominantly inherited disorder characterized mainly by ataxia, spasticity and small pupils that respond poorly to light. More detailed information about the symptoms, causes, and treatments of Ataxia spastic congenital miosis is available below. [wrongdiagnosis online 2009]
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- External Links Related to Ataxia Congenital Miosis Syndrome
- Wikipedia
- Merck
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- PubMed (National Library of Medicine)
- NGC (National Guideline Clearinghouse)
- Medscape (eMedicine)
- Harrison's Online (accessmedicine)
- NEJM (The New England Journal of Medicine)