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Fucosidosis type 1

Fucosidosis type 1: Introduction

Fucosidosis type 1: A rare biochemical disorder involving deficiency of an enzyme (alpha-fucosidase) which results in accumulation of certain chemicals (glycosphingolipids) in the central nervous system and other body tissues. It is an infantile form of fucosidosis which starts early and rapidly progresses to early death. More detailed information about the symptoms, causes, and treatments of Fucosidosis type 1 is available below.

Symptoms of Fucosidosis type 1

Wrongly Diagnosed with Fucosidosis type 1?

Fucosidosis type 1: Related Patient Stories

Fucosidosis type 1: Deaths

Read more about Deaths and Fucosidosis type 1.

Fucosidosis type 1: Complications

Review possible medical complications related to Fucosidosis type 1:

Causes of Fucosidosis type 1

Read more about causes of Fucosidosis type 1.

Disease Topics Related To Fucosidosis type 1

Research the causes of these diseases that are similar to, or related to, Fucosidosis type 1:

Fucosidosis type 1: Animations

Statistics for Fucosidosis type 1

Fucosidosis type 1: Broader Related Topics

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Definitions of Fucosidosis type 1:

Fucosidosis type 1 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Fucosidosis type 1, or a subtype of Fucosidosis type 1, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

 

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