Fructose-1-phosphate aldolase deficiency, hereditary

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

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

Wrongly Diagnosed with 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:

Coma
Intestinal hemorrhage
Liver damage if untreated (see Liver symptoms)
Small intestine damage if untreated
Kidney damage if untreated
more complications...»

Causes of 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:

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...read more »

Statistics for Fructose-1-phosphate aldolase deficiency, hereditary

Fructose-1-phosphate aldolase deficiency, hereditary: Broader Related Topics

Genetic conditions
Metabolic conditions
Congenital conditions - metabolic disorders
Congenital conditions
more types...»

Types 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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