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What is Methylcobalamin deficiency, cbl E complementation type?

What is Methylcobalamin deficiency, cbl E complementation type?

  • Methylcobalamin deficiency, cbl E complementation type: An inherited organic acid disorder where an enzyme deficiency (cbl E) impairs the body's ability to break down cobalamin in the diet. This results in a buildup of homocystine which results in harmful affects.

Methylcobalamin deficiency, cbl E complementation type: Introduction

Types of Methylcobalamin deficiency, cbl E complementation type:

Broader types of Methylcobalamin deficiency, cbl E complementation type:

What causes Methylcobalamin deficiency, cbl E complementation type?

Causes of Methylcobalamin deficiency, cbl E complementation type: see causes of Methylcobalamin deficiency, cbl E complementation type

What are the symptoms of Methylcobalamin deficiency, cbl E complementation type?

Symptoms of Methylcobalamin deficiency, cbl E complementation type: see symptoms of Methylcobalamin deficiency, cbl E complementation type

Methylcobalamin deficiency, cbl E complementation type: Testing

Misdiagnosis: see misdiagnosis and Methylcobalamin deficiency, cbl E complementation type.

How is it treated?

Doctors and Medical Specialists for Methylcobalamin deficiency, cbl E complementation type: Medical Geneticist ; see also doctors and medical specialists for Methylcobalamin deficiency, cbl E complementation type.
Treatments for Methylcobalamin deficiency, cbl E complementation type: see treatments for Methylcobalamin deficiency, cbl E complementation type

Name and Aliases of Methylcobalamin deficiency, cbl E complementation type

Main name of condition: Methylcobalamin deficiency, cbl E complementation type

Other names or spellings for Methylcobalamin deficiency, cbl E complementation type:

vitamin B12-responsive homocytsinuria, cbIE type, homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cbIE complementation type, Methylcobalamin deficiency type cbl E

 

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