About Biotinidase Deficiency

Biotinidase Deficiency, also known as late-onset multiple carboxylase deficiency, is related to biotin deficiency and holocarboxylase synthetase deficiency, and has symptoms including apnea, ataxia and diarrhea. An important gene associated with Biotinidase Deficiency is BTD (Biotinidase), and among its related pathways/superpathways are Metabolism and Diseases of glycosylation. The drugs Folic acid and Biotin have been mentioned in the context of this disorder. Affiliated tissues include skin, brain and eye, and related phenotypes are organic aciduria and metabolic ketoacidosis

Major Symptoms of Biotinidase Deficiency

Biotinidase deficiency, also known as biotin deficiency, is a rare genetic disorder characterized by a deficiency in the enzyme biotinidase. This condition results in the inability to break down biotin, a essential nutrient found in a variety of plant and animal foods, leading to various symptoms. Some of the major symptoms of biotinidase deficiency include:

Suitable Lifestyle for People with Biotinidase Deficiency

Biotinidase deficiency is an inherited enzyme deficiency that primarily affects children and adolescents. Because this is a serious condition, people with Biotinidase deficiency need to pay special attention to their lifestyle to help maintain good health. First, these people should avoid foods that may be high in calories and fat, such as fried foods, desserts, and high-fat meats. Secondly, bad habits such as drinking and smoking should be avoided as these can have a negative impact on health. In addition, attention should be paid to maintaining appropriate movement and exercise to help maintain good health. In summary, people with Biotinidase deficiency need to pay special attention to their lifestyle to help maintain good health. It's best to consult a doctor for more specific advice.

Other Diseases

Creatine Deficiency Syndrome due to AGAT DeficiencyIgA DeficiencyProtein C DeficiencyVitamin B12 DeficiencyLRBA DeficiencyNGLY1 DeficiencyAldosterone DeficiencyProlidase DeficiencyProtein S DeficiencyCoenzyme Q10 DeficiencyTranscobalamin DeficiencyHIBCH DeficiencyVitamin D Deficiency5-oxoprolinase DeficiencyProopiomelanocortin DeficiencyAntithrombin III DeficiencyVitamin A DeficiencyGATA2 DeficiencyVitamin K DeficiencyDNA Ligase IV Deficiency