- ... disorder. Learn more about the gene associated with Carnitine-acylcarnitine translocase deficiency SLC25A20 Inheritance This condition is inherited in an ...
- ... other tissues. Health Conditions Related to Genetic Changes Carnitine-acylcarnitine translocase deficiency At least 27 mutations in the SLC25A20 gene ...
- ... published></health-condition-summary><health-condition-summary ><name >Carnitine-acylcarnitine translocase deficiency</name><ghr-page >https://medlineplus.gov/genetics/condition/ ...
- ... Leukoencephalopathy with vanishing white matter CACT deficiency, see Carnitine-acylcarnitine translocase deficiency CADASIL, see Cerebral autosomal dominant arteriopathy with subcortical ...
- ... topic><topic ><url >https://medlineplus.gov/genetics/condition/carnitine-acylcarnitine-translocase-deficiency</url><title >Carnitine-acylcarnitine translocase deficiency</title><other_ ...
- ... Profound nonketotic hypoglycemia mimics other FAO defects. SLC25A20 Carnitine-acylcarnitine translocase deficiency (OMIM 212138 ) AR AR = autosomal recessive ; FAO = fatty ...
- Lipids include fats, oils, and cholesterol. Disorders like Gaucher disease and Tay-Sachs cause problems with how your body uses lipids. Read more. ... Metabolism is ...
- Mitochondria make energy for your cells. Diseases can affect mitochondria, often causing nerve and muscle problems. Find out more. ... Metabolism is the process your ...
- Your newborn infant has screening tests before leaving the hospital. Get the facts about these tests and what you should expect. ... Your newborn infant has screening ...
- ... 20320. Citation on PubMed Ramsay RR, Zammit VA. Carnitine ... II deficiency: a clinical, biochemical, and molecular review. Lab Invest. ...
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