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Maple syrup urine disease - Genetics Home Reference

Maple syrup urine disease - Genetics Home Reference



04/24/2014 08:32 AM EDT
Genetics Home Reference: your guide to understanding genetic conditions
Source: National Library of Medicine - NIH


Genetics Home Reference: your guide to understanding genetic conditions



Maple syrup urine disease

Reviewed December 2013

What is maple syrup urine disease?

Maple syrup urine disease is an inherited disorder in which the body is unable to process certain protein building blocks (amino acids) properly. The condition gets its name from the distinctive sweet odor of affected infants' urine. Beginning in early infancy, this condition is characterized by poor feeding, vomiting, lack of energy (lethargy), and developmental delay. If untreated, maple syrup urine disease can lead to seizures, coma, and death.
Maple syrup urine disease is often classified by its pattern of signs and symptoms. The most common and severe form of the disease is the classic type, which becomes apparent soon after birth. Variant forms of the disorder become apparent later in infancy or childhood and are typically milder, but they still involve developmental delay and other medical problems if not treated.

How common is maple syrup urine disease?

Maple syrup urine disease affects an estimated 1 in 185,000 infants worldwide. The disorder occurs much more frequently in the Old Order Mennonite population, with an estimated incidence of about 1 in 380 newborns.

What genes are related to maple syrup urine disease?

Mutations in the BCKDHABCKDHBDBT, and DLD genes can cause maple syrup urine disease. These four genes provide instructions for making proteins that work together as a complex. The protein complex is essential for breaking down the amino acids leucine, isoleucine, and valine, which are present in many kinds of food (particularly protein-rich foods such as milk, meat, and eggs).
Mutations in any of these four genes reduce or eliminate the function of the protein complex, preventing the normal breakdown of leucine, isoleucine, and valine. As a result, these amino acids and their byproducts build up in the body. Because high levels of these substances are toxic to the brain and other organs, their accumulation leads to the serious medical problems associated with maple syrup urine disease.
Read more about the BCKDHABCKDHBDBT, and DLD genes.

How do people inherit maple syrup urine disease?

This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not show signs and symptoms of the condition.

Where can I find information about diagnosis or management of maple syrup urine disease?

These resources address the diagnosis or management of maple syrup urine disease and may include treatment providers.
You might also find information on the diagnosis or management of maple syrup urine disease inEducational resources and Patient support.
General information about the diagnosis and management of genetic conditions is available in the Handbook. Read more about genetic testing, particularly the difference between clinical tests and research tests.
To locate a healthcare provider, see How can I find a genetics professional in my area? in the Handbook.

Where can I find additional information about maple syrup urine disease?

You may find the following resources about maple syrup urine disease helpful. These materials are written for the general public.
You may also be interested in these resources, which are designed for healthcare professionals and researchers.

What other names do people use for maple syrup urine disease?

  • BCKD deficiency
  • branched-chain alpha-keto acid dehydrogenase deficiency
  • branched-chain ketoaciduria
  • ketoacidemia
  • MSUD
For more information about naming genetic conditions, see the Genetics Home Reference Condition Naming Guidelines and How are genetic conditions and genes named? in the Handbook.

What if I still have specific questions about maple syrup urine disease?

Where can I find general information about genetic conditions?

What glossary definitions help with understanding maple syrup urine disease?

You may find definitions for these and many other terms in the Genetics Home Reference Glossary.
References (7 links)

The resources on this site should not be used as a substitute for professional medical care or advice. Users seeking information about a personal genetic disease, syndrome, or condition should consult with a qualified healthcare professional. See How can I find a genetics professional in my area? in the Handbook.

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