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Fructose-1-phosphate aldolase deficiency, hereditary

Fructose-1-phosphate aldolase deficiency, hereditary: Introduction

Fructose-1-phosphate aldolase deficiency, hereditary: An inherited metabolic disorder where deficiency of the enzyme fructose-1-phsophate aldolase prevents fructose being metabolized resulting in fructose intolerance. More detailed information about the symptoms, causes, and treatments of Fructose-1-phosphate aldolase deficiency, hereditary is available below.

Symptoms of Fructose-1-phosphate aldolase deficiency, hereditary

See full list of 25 symptoms of Fructose-1-phosphate aldolase deficiency, hereditary

Fructose-1-phosphate aldolase deficiency, hereditary: Complications

Review possible medical complications related to Fructose-1-phosphate aldolase deficiency, hereditary:

Disease Topics Related To Fructose-1-phosphate aldolase deficiency, hereditary

Research the causes of these diseases that are similar to, or related to, Fructose-1-phosphate aldolase deficiency, hereditary:

Medical Textbooks Online about Fructose-1-phosphate aldolase deficiency, hereditary

Medical Books Excerpts
 

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

Wrongly Diagnosed with Fructose-1-phosphate aldolase deficiency, hereditary?

Misdiagnosis and Fructose-1-phosphate aldolase deficiency, hereditary

Vitamin B12 deficiency under-diagnosed: The condition of Vitamin B12 deficiency is a possible misdiagnosis of various conditions, such as multiple sclerosis (see symptoms of multiple sclerosis). See symptoms of Vitamin B12 deficiency or misdiagnosis of multiple sclerosis....read more »

Read more about Misdiagnosis and Fructose-1-phosphate aldolase deficiency, hereditary

Causes of Fructose-1-phosphate aldolase deficiency, hereditary

Read more about causes of Fructose-1-phosphate aldolase deficiency, hereditary.

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Definitions of Fructose-1-phosphate aldolase deficiency, hereditary:

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Fructose-1-phosphate aldolase deficiency, hereditary as a "rare disease".
Source - Orphanet


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