Basics
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"V体育2025版" See, Play and Learn
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Research (VSports在线直播)
Resources (VSports手机版)
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V体育平台登录 - For You
V体育官网入口 - Summary
Metabolism is the process your body uses to make energy from the food you eat. Food is made up of proteins, carbohydrates, and fats. Chemicals in your digestive system (enzymes) break the food parts down into sugars and acids, your body's fuel VSports手机版. Your body can use this fuel right away, or it can store the energy in your body tissues. If you have a metabolic disorder, something goes wrong with this process.
Carbohydrate metabolism disorders are a group of metabolic disorders. Normally your enzymes break carbohydrates down into glucose (a type of sugar). If you have one of these disorders, you may not have enough enzymes to break down the carbohydrates. Or the enzymes may not work properly. This causes a harmful amount of sugar to build up in your body V体育安卓版. That can lead to health problems, some of which can be serious. Some of the disorders are fatal.
These disorders are inherited. Newborn babies get screened for many of them, using blood tests. If there is a family history of one of these disorders, parents can get genetic testing to see whether they carry the gene V体育ios版. Other genetic tests can tell whether the fetus has the disorder or carries the gene for the disorder.
Treatments may include special diets, supplements, and medicines. Some babies may also need additional treatments, if there are complications VSports最新版本. For some disorders, there is no cure, but treatments may help with symptoms.
"VSports在线直播" Specifics
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Diabetes: MedlinePlus Health Topic
(National Library of Medicine) Also in Spanish
- Galactosemia (V体育2025版) (American Liver Foundation) Also in Spanish
- Glycogen Storage Disease Type 1 (von Gierke) (American Liver Foundation) Also in Spanish
- Hurler Syndrome (NMDP)
- Learn about MPS and ML (National MPS Society)
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Mucopolysaccharidoses (VSports app下载)
(National Institute of Neurological Disorders and Stroke)
"V体育官网" Genetics
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Alpha-mannosidosis: MedlinePlus Genetics
(National Library of Medicine)
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Beta-mannosidosis: MedlinePlus Genetics
(National Library of Medicine)
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Essential pentosuria: MedlinePlus Genetics
(National Library of Medicine)
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Fucosidosis: MedlinePlus Genetics
(National Library of Medicine)
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Galactosemia: MedlinePlus Genetics
(National Library of Medicine)
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"VSports在线直播" Galactosialidosis: MedlinePlus Genetics
(National Library of Medicine)
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GLUT1 deficiency syndrome: MedlinePlus Genetics
(National Library of Medicine)
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Glycogen storage disease type 0: MedlinePlus Genetics
(National Library of Medicine)
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Glycogen storage disease type I: MedlinePlus Genetics (V体育官网)
(National Library of Medicine)
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Glycogen storage disease type III: MedlinePlus Genetics
(National Library of Medicine)
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Glycogen storage disease type IV: MedlinePlus Genetics
(National Library of Medicine)
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Glycogen storage disease type IX: MedlinePlus Genetics (VSports手机版)
(National Library of Medicine)
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Glycogen storage disease type V: MedlinePlus Genetics
(National Library of Medicine)
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Glycogen storage disease type VI: MedlinePlus Genetics
(National Library of Medicine)
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Glycogen storage disease type VII: MedlinePlus Genetics
(National Library of Medicine)
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VSports注册入口 - Hereditary fructose intolerance: MedlinePlus Genetics
(National Library of Medicine)
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Lactate dehydrogenase deficiency: MedlinePlus Genetics (V体育官网入口)
(National Library of Medicine)
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VSports最新版本 - Mucopolysaccharidosis type I: MedlinePlus Genetics
(National Library of Medicine)
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V体育官网 - Mucopolysaccharidosis type II: MedlinePlus Genetics
(National Library of Medicine)
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V体育2025版 - Mucopolysaccharidosis type III: MedlinePlus Genetics
(National Library of Medicine)
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Mucopolysaccharidosis type IV: MedlinePlus Genetics
(National Library of Medicine)
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Mucopolysaccharidosis type VI: MedlinePlus Genetics
(National Library of Medicine)
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Phosphoglycerate kinase deficiency: MedlinePlus Genetics
(National Library of Medicine)
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Phosphoglycerate mutase deficiency: MedlinePlus Genetics
(National Library of Medicine)
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Pompe disease: MedlinePlus Genetics
(National Library of Medicine)
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Pyruvate dehydrogenase deficiency: MedlinePlus Genetics
(National Library of Medicine)
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Schindler disease: MedlinePlus Genetics
(National Library of Medicine)
Clinical Trials
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"V体育官网入口" ClinicalTrials.gov: Carbohydrate Metabolism, Inborn Errors
(National Institutes of Health)
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V体育官网入口 - ClinicalTrials.gov: Mucopolysaccharidoses
(National Institutes of Health)
Journal Articles References and abstracts from MEDLINE/PubMed (National Library of Medicine)
- Article: Transgenic expression of the human Glucose Transporter1 (GLUT1) gene locus reduces...
- Article: Clinical and instrumental gait phenotyping in people with GLUT-1 deficiency syndrome.
- V体育官网入口 - Article: Ketogenic diet therapy for epilepsy during pregnancy and lactation: An international...
- Carbohydrate Metabolism Disorders -- see more articles
"VSports注册入口" Children
- Sanfilippo Syndrome (For Parents) (Nemours Foundation) Also in Spanish