Deficiency refers to a lack or insufficiency of essential nutrients, substances, or elements required for the proper functioning of the body. It can occur when the body does not receive an adequate supply of vitamins, minerals, proteins, fats, carbohydrates, or other essential compounds necessary for maintaining health and well-being. Deficiencies can arise due to various ... 【More】
Deficiency refers to a lack or insufficiency of essential nutrients, substances, or elements required for the proper functioning of the body. It can occur when the body does not receive an adequate supply of vitamins, minerals, proteins, fats, carbohydrates, or other essential compounds necessary for maintaining health and well-being. Deficiencies can arise due to various factors, including poor dietary intake, malabsorption disorders, certain medical conditions, or increased nutritional requirements during growth, pregnancy, or illness. Common deficiencies include iron deficiency anemia, vitamin D deficiency, vitamin B12 deficiency, and iodine deficiency disorders. Treatment typically involves addressing the underlying cause and may include dietary changes, supplementation, or medical interventions as necessary. 【Less】
AGAT Deficiency Syndrome: Dietary and Lifestyle Guidance disease
Cerebral Creatine Deficiency Syndrome 3, also known as arginine:glycine amidinotransferase deficiency, is related to cerebral creatine deficiency syndrome 1 and type 2 diabetes mellitus. An important gene associated with Cerebral Creatine Deficiency Syndrome 3 is GATM (Glycine Amidinotransferase), and among its related pathways/superpathways ...
HSD10 Mitochondrial Disease: Symptoms and Lifestyle disease
Hsd10 Mitochondrial Disease, also known as 2-methyl-3-hydroxybutyryl-coa dehydrogenase deficiency, is related to syndromic x-linked intellectual disability type 10 and 2-methylbutyryl-coa dehydrogenase deficiency, and has symptoms including muscle spasticity, seizures and agitation. An important gene associated with Hsd10 Mitochondrial ...
Understanding 3MCP Deficiency and Its Impact disease
3-Methylcrotonyl-Coa Carboxylase Deficiency, also known as 3-methylcrotonylglycinuria, is related to abdominal obesity-metabolic syndrome 1 and reye syndrome, and has symptoms including muscular hypotonia, muscular atrophy and feeding difficulties. An important gene associated with 3-Methylcrotonyl-Coa Carboxylase Deficiency is MCCC1 ...
Managing Cholesterol in HMGCS2 Deficiency disease
3-Hydroxy-3-Methylglutaryl-Coa Synthase-2 Deficiency, also known as 3-hydroxy-3-methylglutaryl-coa synthase deficiency, is related to hmg coa synthetase deficiency and hypertriglyceridemia 1, and has symptoms including diarrhea and vomiting. An important gene associated with 3-Hydroxy-3-Methylglutaryl-Coa Synthase-2 Deficiency is HMGCS2 ...