Skip navigation

Refine by Type

Results 1 - 10 of 13 for "3-Methylglutaconic" aciduria type 2
  1. Genetics Home Reference: Barth syndrome From the National Institutes of Health (National Library of Medicine)  
    ... gov Research studies OMIM Genetic disorder catalog Conditions > Barth syndrome On this page: Description Genetic changes Inheritance Diagnosis ... names Glossary definitions Reviewed July 2014 What is Barth syndrome? Barth syndrome is a rare condition characterized by ...
  2. Barth Syndrome (BTHS) From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    NINDS Barth Syndrome Information Page Table of Contents (click to jump to sections) What is Barth Syndrome? Is there any ... is being done? Clinical Trials Organizations What is Barth Syndrome? Barth syndrome (BTHS) is a rare, genetic disorder ...
  3. Metabolic Disorders (National Library of Medicine)  
    Metabolism is the process your body uses to get or make energy from the food you eat. Food is made up of proteins, carbohydrates, and fats. Chemicals in your digestive ...
  4. Causes of Cardiomyopathy (Children's Cardiomyopathy Foundation)  
    ... syndrome, Pompe disease, fatty acid oxidation defect or Barth syndrome. Most often, symptoms of these disorders present early ... deficiency, VCHAD, LCHAD, LCAD, MCAD), Pompe disease and Barth syndrome. When the demand for energy exceeds what the ...
  5. National Institute of Neurological Disorders and Stroke (National Institute of Neurological Disorders and Stroke)  
    ... Deficit- Hyperactivity Disorder Autism Autonomic Dysfunction Back Pain Barth Syndrome Batten Disease Behcet's Disease Bell's Palsy Benign Essential ...
  6. Cardiomyopathy (National Library of Medicine)  
    Cardiomyopathy is the name for diseases of the heart muscle. These diseases enlarge your heart muscle or make it thicker and more rigid than normal. In rare cases, ...
  7. What's Cardiomyopathy (Children's Cardiomyopathy Foundation)  
    ... a genetic disorder such as fatty acid oxidation, Barth syndrome, or Noonan syndrome. Cardiomyopathy can also be a ...
  8. Genetic Brain Disorders (National Library of Medicine)  
    A genetic brain disorder is caused by a variation or a mutation in a gene. A variation is a different form of a gene. A mutation is a change in a gene. ...
  9. Genetics Home Reference: Cardiomyopathy From the National Institutes of Health (National Library of Medicine)  
    ... on Genetics Home Reference: arrhythmogenic right ventricular cardiomyopathy Barth syndrome Danon disease dilated cardiomyopathy with ataxia syndrome DMD- ...
  10. Newborn Screening (National Library of Medicine)  
    Your newborn infant has screening tests before leaving the hospital. There may be different tests depending on the state where you live. They include Tests ...
previous · 1 · 2 · next