What Is Vlcad?

What are the symptoms of Vlcad?

Signs and symptoms of VLCAD deficiency typically appear during infancy or early childhood and can include low blood sugar (hypoglycemia), lack of energy (lethargy), and muscle weakness.

Affected individuals are also at risk for serious complications such as liver abnormalities and life-threatening heart problems..

What is a Vlcad carrier?

VLCAD deficiency is inherited in an autosomal recessive manner. This means that to be affected, a person must have a mutation in both copies of the responsible gene in each cell . The parents of an affected person usually each carry one mutated copy of the gene and are referred to as carriers .

What is Ryders genetic condition?

VLCAD deficiency is a condition in which the body is unable to properly breakdown certain fats (called very long-chain fatty acids) into energy, particularly during periods without food (fasting).

Can you live with Vlcad?

Along with those symptomatic infants who make it to adulthood, some adults with VLCAD deficiency will have a milder form of the disorder that is only diagnosed later in life. When this occurs, the adults are typically less likely to experience these life-threatening issues and are able to live mostly normal lives.

Is Vlcad life threatening?

The lifespan of people with VLCAD deficiency varies. The severe form of this condition which begins during infancy can cause life-threatening cardiomyopathy or heart rhythm disorders. However, early diagnosis and proper treatment play an important role in preventing these serious health complications.

How is Vlcad treated?

Treatment. Management of VLCAD deficiency is focused primarily on preventing acute episodes of low blood sugar (hypoglycemia). This process includes avoiding fasting and using a very low-fat, high-carbohydrate diet, with frequent feeding.

What can you eat with Vlcad?

Children with VLCAD should have a starchy snack (such as bread, cereal, and rice) before bed and another during the night. They need another snack first thing in the morning. Raw cornstarch mixed with water, milk, or other drink is a good source of long- lasting energy.

What causes Mcadd?

MCADD is caused by a fault in the gene that provides the instructions to make an enzyme called medium-chain acyl-CoA dehydrogenase (MCAD). This genetic fault causes the enzyme to either not work properly or be missing entirely, which means the body cannot fully break down fat to release energy.

What is MCAD deficiency?

Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency is an inherited disorder that prevents your body from breaking down certain fats and converting them into energy. As a result, the level of sugar in your blood can drop dangerously low (hypoglycemia).

Is coconut oil a long chain fatty acid?

Coconut oil is a highly saturated oil (about 90%), and 60% of its total fatty acid composition are medium-chain fatty acid (MCFA) with a chain length of 6 to 12 carbon atoms (Bhatnagar et al., 2009), which are absorbed directly into the portal circulation without re-esterification in intestinal cells (Ferreira et al., …