What are the symptoms of Vlcad?
Signs of a VLCAD include:
- Sleeping longer or more often.
- Tiredness.
- Behavior changes.
- Muscle weakness (known as hypotonia)
- Irritability.
- Poor appetite.
- Fever.
- Vomiting.
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.
How do you get Vlcad?
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 .
Can you live a normal life 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 hereditary?
How do you test for Vlcad?
This testing may include specialized tests performed on a sample of blood, urine, skin cells , muscle, and/or liver tissue . Genetic testing for changes ( mutations ) in the ACADVL gene can confirm the diagnosis. GeneReview’s Web site offers more specific information about the diagnosis of VLCAD deficiency.
What do people with Vlcad eat?
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.
Can you live a normal life with VLCAD?
What do people with VLCAD eat?
What Rare Disease Does Ryder have?
VLCAD deficiency
Our Story. At birth, Ryder K Wharton was diagnosed with a rare condition named VLCAD. VLCAD deficiency is a rare condition in which the body is unable to properly breakdown certain fats into energy, particularly during periods without food.
Is VLCAD hereditary?
