Hematoporphyria Chronic

Chronic hematoporphyria: symptoms, diagnosis and treatment

Chronic hematoporphyria, also known as haematoporphyria chronica, is a rare inherited disease associated with impaired synthesis of heme, the main component of hemoglobin. This disorder leads to the accumulation of heme precursors in the blood and organs, leading to various symptoms and complications.

Symptoms of hematoporphyria chronica may include feeling tired, weak, abdominal pain, increased sensitivity to sunlight and changes in skin color. In some cases, episodes of painful damage to the nervous system, such as peripheral neuritis and neuropathy, may occur.

Diagnosis of chronic hematoporphyria is based on analysis of the level of heme precursors in the blood and detection of mutations in the genes responsible for heme synthesis. It is important to establish an accurate diagnosis, since chronic hematoporphyria can be misdiagnosed as other diseases such as psoriasis and solar dermatitis.

Treatment for hematoporphyria chronica includes managing symptoms, such as pain and changes in skin color, and treating complications, such as nerve damage. However, there is no specific treatment that can completely cure this disease. Some patients may receive regular blood transfusions to reduce the levels of heme precursors in the blood.

It is also important to take precautions to avoid worsening your symptoms. This may include avoiding sunlight, certain medications, and alcohol, which can trigger episodes of nervous system damage.

In conclusion, hematoporphyria chronica is a rare genetic disorder that can have serious health consequences. It is important to receive an accurate diagnosis and treatment to manage symptoms and avoid complications. If you suspect chronic hematoporphyria, consult your doctor for further research and consultation.

Hematoporphya is a rare genetic disorder that is characterized by excess production of porphyrin in the body. This leads to changes in skin and hair color, as well as other symptoms such as fatigue, headaches and stomach pain. Hematoportria can have different forms, including a chronic form. In this article we will look at hemachorinmia as a genetic disorder. And how to treat such genetic disorders of the body. Blood diseases are varied: some affect the production of white blood cells (for example, leukemia), others affect the formation of platelets (thrombocytopenia or thrombophilia). But the most common disorder in this area is associated with the activity of the porphyrin ring, which is responsible for the formation of red blood cells (erythrocytes). The complexity of understanding the genetic nature of hematoporia lies not only in choosing the correct treatment when making clinical decisions, but also in determining and confirming biological