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Spongy degeneration of central nervous system
- ... Testing Registry: Mild Canavan disease Genetic Testing Registry: Spongy degeneration of central nervous system Canavan disease National Organization for Rare Disorders (NORD) ...
- Canavan disease is a condition that affects how the body breaks down and uses aspartic acid . ... Canavan disease is passed down (inherited) through families. It is more common among the Ashkenazi Jewish population than ...
- Leukodystrophies (National Library of Medicine)What are leukodystrophies? Leukodystrophies are a group of rare genetic disorders that affect the central nervous system (CNS). The CNS is made up of your ...
- ... in the ASPA gene are known to cause Canavan disease, which is a rare inherited disorder that affects ... two major forms of this condition: neonatal/infantile Canavan disease, which is the most common and most severe ...
- Leukodystrophies/Clinical Trials ... Leukodystrophies ... National Institutes of Health ... From the National Institutes of Health
- ... neuropathy Polycystic kidney disease Beta thalassemia Bloom syndrome Canavan disease PMM2 -congenital disorder of glycosylation , also called PMM2 - ...
- ... risk of having babies with Tay-Sachs or Canavan disease. African Americans, who may risk passing sickle-cell ...
- ... familial macrocephaly (family tendency toward large head size) Canavan disease (condition that affects how the body breaks down ...
- ... urine amino acids may be due to: Alkaptonuria Canavan disease Cystinosis Cystathioninuria Fructose intolerance Galactosemia Hartnup disease Homocystinuria ...