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Spinal Muscular Atrophy type I

Spinal Muscular Atrophy type I: Introduction

A type of spinal muscular atrophy which is a progressive genetic motor neuron disease involving the nerves and muscles. The condition is relatively rare and is characterized by muscle weakness which leads to structural deformities and loss or reduced capability of normal body movements. SMA type I is the most debilitating form as muscular weakness is evident at birth and diagnosis usually occurs within the first three months. Also called Werdnig-Hoffmann Disease or infantile SMA.

Symptoms of Spinal Muscular Atrophy type I

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Spinal Muscular Atrophy type I: Complications

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Disease Topics Related To Spinal Muscular Atrophy type I

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Medical Textbooks Online about Spinal Muscular Atrophy type I

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Book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.

Wrongly Diagnosed with Spinal Muscular Atrophy type I?

Spinal Muscular Atrophy type I: Marketplace Products, Discounts & Offers

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News Archives for Spinal Muscular Atrophy type I

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Evidence Based Medicine Research for Spinal Muscular Atrophy type I

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Videos for Spinal Muscular Atrophy type I

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Prognosis for Spinal Muscular Atrophy type I

Prognosis for Spinal Muscular Atrophy type I: Poor. Death usually by 2 years.

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Reseach about Spinal Muscular Atrophy type I

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Statistics for Spinal Muscular Atrophy type I

Spinal Muscular Atrophy type I: Broader Related Topics

Types of Spinal Muscular Atrophy type I

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Definitions of Spinal Muscular Atrophy type I:

Spinal Muscular Atrophy type I is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Spinal Muscular Atrophy type I, or a subtype of Spinal Muscular Atrophy type I, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)


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