About Succinic Semialdehyde Dehydrogenase Deficiency

Succinic Semialdehyde Dehydrogenase Deficiency, also known as 4-hydroxybutyric aciduria, is related to gaba aminotransferase deficiency and gaba-transaminase deficiency, and has symptoms including ataxia, seizures and absence seizures. An important gene associated with Succinic Semialdehyde Dehydrogenase Deficiency is ALDH5A1 (Aldehyde Dehydrogenase 5 Family Member A1), and among its related pathways/superpathways are Metabolism and Regulation of expression of SLITs and ROBOs. The drugs SGS-742 and Protective Agents have been mentioned in the context of this disorder. Affiliated tissues include eye, brain and globus pallidus, and related phenotypes are intellectual disability and ataxia

Major Symptoms of Succinic Semialdehyde Dehydrogenase Deficiency

Succinic semialdehyde dehydrogenase deficiency is a rare genetic disorder that primarily affects the liver and kidneys. The major symptoms include jaundice, itching, and jaundice again.

Suitable Lifestyle for People with Succinic Semialdehyde Dehydrogenase Deficiency

Suitable lifestyle options for people suffering from Succinic semialdehyde dehydrogenase deficiency include:

1. Maintain a healthy lifestyle: maintain adequate sleep, a balanced diet, appropriate exercise, and reduce stress.

2. Avoid harmful substances: Avoid bad habits such as drinking and smoking, as well as exposure to harmful environmental substances.

3. Maintain good personal hygiene: wash hands frequently, keep clean, etc.

4. Pay attention to mental health: maintain good communication with family and friends, and seek psychological help.

5. Follow your doctor's advice: Carry out treatment and monitoring under the guidance of your doctor, and follow your doctor's advice.

6. Participate in social activities: Participate in some social activities, such as participating in community activities, sports, etc. , to increase social connections and support each other.

Other Diseases

Phosphoglycerate Dehydrogenase DeficiencyPyruvate Dehydrogenase Deficiency3-hydroxyacyl-CoA Dehydrogenase DeficiencyIsobutyryl-CoA Dehydrogenase Deficiency17-beta-hydroxysteroid Dehydrogenase X DeficiencyFatty Aldehyde Dehydrogenase DeficiencyMedium-chain Acyl-CoA Dehydrogenase DeficiencyShort-chain Acyl-CoA Dehydrogenase DeficiencyVery Long-chain Acyl-CoA Dehydrogenase DeficiencyLong-chain 3-hydroxyacyl-coenzyme A Dehydrogenase DeficiencyCreatine Deficiency Syndrome due to AGAT DeficiencyIgA DeficiencyGATA2 DeficiencyAntithrombin III Deficiency5-oxoprolinase DeficiencyProopiomelanocortin DeficiencyVitamin K DeficiencyVitamin D DeficiencyVitamin B12 DeficiencyProlidase Deficiency