Primary carnitine deficiency: Difference between revisions

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Typically, initial signs  of this disorder occur during infancy or early childhood and often include brain function abnormalities
Typically, initial signs  of this disorder occur during infancy or early childhood and often include brain function abnormalities


==== Heart ====
* [[Cardiomyopathy]]
==== Neuroloogic ====
==== Neuroloogic ====


* [[Encephalopathy]]
* [[Encephalopathy]]
==== Heart ====
* [[Cardiomyopathy]]


=== Laboratory Findings ===
=== Laboratory Findings ===

Revision as of 15:57, 6 August 2012

Primary carnitine deficiency
Carnitine
ICD-10 E71.3
ICD-9 277.81
OMIM 212140
DiseasesDB 31103

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Primary carnitine deficiency is a condition that prevents the body from using fats for energy, particularly during periods without food. Carnitine, a natural substance acquired mostly through diet, is used by cells to process fats and produce energy. People with primary carnitine deficiency have defective proteins called carnitine transporters, which bring carnitine into cells and prevent its escape from the body.

Historical Perspective

The current understanding of primary carnitine deficiency has been greatly influenced by the research of Doctors Susan C. Winter and Neil Buist. Dr. Winter was one of the first doctors in the United States to begin treating inborn errors of metabolism with intravenous carnitine.

Pathophysiology

There is a decrease in the transport function as a result carnitine is lost from the body. Cells are not supplied with an adequate amount of carnitine. Without carnitine, fats cannot be processed correctly and are not converted into energy, which can lead to characteristic signs and symptoms of this disorder.

Genetics

Mutations in the SLC22A5 gene lead to the production of defective carnitine transporters. This condition is inherited in an autosomal recessive pattern.

Differentiating from other Diseases

This condition is sometimes mistaken for Reye syndrome, a severe disorder that develops in children while they appear to be recovering from viral infections such as chickenpox or flu. Most cases of Reye syndrome are associated with the use of aspirin during these viral infections.

Epidemiology and Demographics

On the average, primary carnitine deficiency affects 1 in every 40,000 live births in Japan and 1 in every 37,000 to 100,000 newborns in Australia. The incidence of this condition in other populations is unknown, but is probably similar to that reported for Japan.

Risk Factors

Natural History, Complications and Prognosis

Serious complications such as heart failure, liver problems, coma, and sudden unexpected death can occur. Acute illness due to primary carnitine deficiency can be triggered by periods of fasting or illnesses such as viral infections, particularly when eating is reduced.

Diagnosis

Symptoms

Physical Examination

Typically, initial signs of this disorder occur during infancy or early childhood and often include brain function abnormalities

Heart

Neuroloogic

Laboratory Findings

Electrolyte and Biomarker Studies

Treatment

Primary carnitine deficiency is sometimes diagnosed in adults and is then thought to be less severe both in symptoms and life expectation. Treatment is usually done by supplementation of L-carnitine after assessing the severity of the deficiency after a muscular biopsy.

References

This article incorporates public domain text from The U.S. National Library of Medicine

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