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Glycogen storage "disease," type II
- Newborn Screening Tests (Nemours Foundation)Newborn Screening/Start Here ... Newborn Screening ... Nemours Foundation ... newborn screening tests, metabolic disorders, genetic disorders, pku, phenylketonuria, ...
- Newborn Screening Tests for Your Baby (March of Dimes Foundation)Newborn Screening/Specifics ... Newborn Screening ... March of Dimes Foundation
- Disease Treatments (American Society of Gene & Cell Therapy)Genes and Gene Therapy/Specifics ... Genes and Gene Therapy ... American Society of Gene & Cell Therapy
- Pompe Disease (National Institute of Neurological Disorders and Stroke)... disease (also known as acid-maltase disease and glycogen storage disease II) is a rare genetic disorder that causes progressive weakness to the heart and skeletal muscles. It is caused by mutations in a ... body uses to break down glycogen, a stored form of sugar used for energy.
- Galactosemia (American Liver Foundation)Carbohydrate Metabolism Disorders/Specifics ... Carbohydrate Metabolism Disorders ... Liver Diseases/Children ... Liver Diseases ... Galactosemia is an inherited disorder ...
- Childhood Hepatocellular Carcinoma (National Cancer Institute)Liver Cancer/Children ... Liver Cancer ... National Cancer Institute ... From the National Institutes of Health ... Childhood hepatocellular carcinoma is a rare type of childhood ...
- Hepatoblastoma (National Cancer Institute)Liver Cancer/Children ... Liver Cancer ... National Cancer Institute ... From the National Institutes of Health ... Hepatoblastoma is the most common type of childhood liver ...