Prenatal Treatment of Methylmalonic Acidemia
Methylmalonic acidemia (MMA) is a rare but serious genetic metabolic disorder that affects the body’s ability to break down certain fats and proteins. This condition…
Homocystinuria Type III: Causes, Symptoms
Homocystinuria type III is a rare metabolic disorder characterized by elevated homocysteine levels in the blood. This condition results from mutations in the MTHFR gene,…
Glutaric Aciduria Type I: Causes, Symptoms, Diagnosis
Glutaric aciduria type I (GA-I) is a rare genetic metabolic disorder characterized by the body's inability to process certain amino acids properly. This condition leads…