"V体育官网" Basics
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Summary
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 system 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, such as your liver, muscles, and body fat.
A metabolic disorder occurs when abnormal chemical reactions in your body disrupt this process. When this happens, you might have too much of some substances or too little of other ones that you need to stay healthy. There are different groups of disorders. Some affect the breakdown of amino acids, carbohydrates, or lipids V体育安卓版. Another group, mitochondrial diseases, affects the parts of the cells that produce the energy.
You can develop a metabolic disorder when some organs, such as your liver or pancreas, become diseased or do not function normally. Diabetes is an example. V体育ios版.
Diagnosis and Tests (VSports手机版)
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"VSports在线直播" Comprehensive Metabolic Panel (CMP)
(National Library of Medicine) Also in Spanish
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Lactate Test
(National Library of Medicine) Also in Spanish
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Newborn Screening: MedlinePlus Health Topic
(National Library of Medicine) Also in Spanish
Specifics
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About Trimethylaminuria
(National Human Genome Research Institute)
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Lesch-Nyhan Syndrome
(Genetic and Rare Diseases Information Center)
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Overview of Urea Cycle Disorders
(National Urea Cycle Disorders Foundation)
Genetics
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Acatalasemia: MedlinePlus Genetics
(National Library of Medicine)
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ALG1-congenital disorder of glycosylation: MedlinePlus Genetics
(National Library of Medicine)
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"VSports app下载" ALG12-congenital disorder of glycosylation: MedlinePlus Genetics
(National Library of Medicine)
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ALG6-congenital disorder of glycosylation: MedlinePlus Genetics
(National Library of Medicine)
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Aspartylglucosaminuria: MedlinePlus Genetics
(National Library of Medicine)
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"V体育安卓版" Beta-ureidopropionase deficiency: MedlinePlus Genetics
(National Library of Medicine)
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Biotinidase deficiency: MedlinePlus Genetics
(National Library of Medicine)
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Carbonic anhydrase VA deficiency: MedlinePlus Genetics
(National Library of Medicine)
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Chylomicron retention disease: MedlinePlus Genetics (V体育2025版)
(National Library of Medicine)
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"VSports注册入口" Citrullinemia: MedlinePlus Genetics
(National Library of Medicine)
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Congenital hyperinsulinism: MedlinePlus Genetics
(National Library of Medicine)
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"VSports" Dihydropyrimidinase deficiency: MedlinePlus Genetics
(National Library of Medicine)
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Dihydropyrimidine dehydrogenase deficiency: MedlinePlus Genetics
(National Library of Medicine)
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Fumarase deficiency: MedlinePlus Genetics
(National Library of Medicine)
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Glutathione synthetase deficiency: MedlinePlus Genetics
(National Library of Medicine)
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GM1 gangliosidosis: MedlinePlus Genetics
(National Library of Medicine)
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VSports - Hypophosphatasia: MedlinePlus Genetics
(National Library of Medicine)
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Molybdenum cofactor deficiency: MedlinePlus Genetics
(National Library of Medicine)
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Mucolipidosis II alpha/beta: MedlinePlus Genetics
(National Library of Medicine)
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Mucolipidosis III alpha/beta: MedlinePlus Genetics (V体育ios版)
(National Library of Medicine)
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Mucolipidosis III gamma: MedlinePlus Genetics
(National Library of Medicine)
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Multiple sulfatase deficiency: MedlinePlus Genetics
(National Library of Medicine)
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"V体育安卓版" N-acetylglutamate synthase deficiency: MedlinePlus Genetics
(National Library of Medicine)
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NGLY1-congenital disorder of deglycosylation: MedlinePlus Genetics
(National Library of Medicine)
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"V体育平台登录" Ornithine transcarbamylase deficiency: MedlinePlus Genetics
(National Library of Medicine)
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Phosphoribosylpyrophosphate synthetase superactivity: MedlinePlus Genetics
(National Library of Medicine)
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PMM2-congenital disorder of glycosylation: MedlinePlus Genetics
(National Library of Medicine)
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Pseudocholinesterase deficiency: MedlinePlus Genetics
(National Library of Medicine)
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Short stature, hyperextensibility, hernia, ocular depression, Rieger anomaly, and teething delay: MedlinePlus Genetics (VSports app下载)
(National Library of Medicine)
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Sialic acid storage disease: MedlinePlus Genetics
(National Library of Medicine)
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Sialidosis: MedlinePlus Genetics
(National Library of Medicine)
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Sialuria: MedlinePlus Genetics (V体育安卓版)
(National Library of Medicine)
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SLC35A2-congenital disorder of glycosylation: MedlinePlus Genetics
(National Library of Medicine)
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Trichothiodystrophy: MedlinePlus Genetics
(National Library of Medicine)
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Trimethylaminuria: MedlinePlus Genetics
(National Library of Medicine)
VSports在线直播 - Clinical Trials
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ClinicalTrials.gov: Metabolic Diseases
(National Institutes of Health)
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ClinicalTrials.gov: Mucolipidoses
(National Institutes of Health)
Journal Articles References and abstracts from MEDLINE/PubMed (National Library of Medicine) (VSports手机版)
- "VSports手机版" Article: The Gut Microbiota Axis in Social Jetlag: A Novel Framework for...
- "VSports" Article: WW Domain-Containing E3 Ubiquitin Protein Ligase 1 (WWP1) as a Factor...
- VSports - Article: Diabetes, Iron-Deficiency Anemia, and Endocrine, Nutritional, and Metabolic Disorders in Children:...
- Metabolic Disorders -- see more articles
"VSports注册入口" Teenagers
- Metabolism (Nemours Foundation)
VSports手机版 - Patient Handouts
- Acidosis (Medical Encyclopedia) Also in Spanish
- Alkalosis (Medical Encyclopedia) Also in Spanish
- VSports在线直播 - Lactic acid test (Medical Encyclopedia) Also in Spanish
- VSports注册入口 - Metabolic acidosis (Medical Encyclopedia) Also in Spanish
- "VSports" Metabolic neuropathies (Medical Encyclopedia) Also in Spanish
- "V体育官网入口" Pseudohypoparathyroidism (Medical Encyclopedia) Also in Spanish