Acute intermittent porphyria is a genetic disease that causes excessive production and secretion of porphyrins, leading to neurological and digestive problems. Environmental factors can trigger acute attacks, but medication and avoiding triggers can reduce symptoms. Symptoms include severe abdominal pain, cramping, diarrhea, nausea, headache, fever, confusion, severe muscle pain, numbness, tingling, and, rarely, seizures or […]
Porphyria Cutanea Tarda is a rare enzyme deficiency that causes sensitivity to sunlight and skin blistering. It is often asymptomatic and caused by an abnormally high demand for heme. Treatment involves avoiding triggers and relieving symptoms. Porphyria Cutanea Tarda is the most common type of the group of enzyme deficiencies classified as porphyrias. It is […]
Porphyria is a group of genetic disorders that affect the nervous system and skin, caused by a buildup of porphyrins in the body. Symptoms vary depending on the type of porphyria, and triggers can include hormonal fluctuations, high levels of iron, viruses, and certain medications. Treatments focus on preventing attacks and lowering porphyrin levels, and […]
