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Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency: Introduction
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency: A rare inherited genetic condition where the body is unable to convert certain fats to energy i.e. there is not enough of a certain enzyme (3-hydroxyacyl-coenzyme A dehydrogenase) which is needed to metabolize a type of fat called long-chain fatty acids. The build-up of these fatty acids in the body causes damage.
More detailed information about the symptoms,
causes, and treatments of Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency is available below.
Symptoms of Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
See full list of 16
symptoms of Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
Wrongly Diagnosed with Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency?
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency: Related Patient Stories
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency: Deaths
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Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency: Complications
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Causes of Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
- The condition is inherited in an autosomal recessive manner
- more causes...»
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Disease Topics Related To Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
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Misdiagnosis and Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
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Read more about Misdiagnosis and Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
Statistics for Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency: Broader Related Topics
Types of Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
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