Congenital and hereditary thrombocytopenia purpura digital illustration

Congenital and hereditary thrombocytopenia purpura Save


ICD-10 code: D69.42

Disease category: D69.4: Other primary thrombocytopenia

Congenital and Hereditary Thrombocytopenia Purpura

Congenital and hereditary thrombocytopenia purpura is a rare blood disorder characterized by low platelet count and abnormal bleeding. This condition is present at birth and is usually inherited from one or both parents. Thrombocytopenia purpura can be congenital, meaning it is caused by genetic mutations, or hereditary, meaning it runs in families.

Individuals with congenital and hereditary thrombocytopenia purpura often experience symptoms such as easy bruising, nosebleeds, and prolonged bleeding from cuts or injuries. The low platelet count makes it difficult for blood to clot properly, leading to these symptoms. It is important for individuals with this condition to take extra precautions to avoid injuries and to inform healthcare professionals about their condition before any medical procedures.

Types of Congenital and Hereditary Thrombocytopenia Purpura:

  1. Wiskott-Aldrich Syndrome (WAS): This inherited disorder affects the immune system and leads to low platelet count, eczema, and recurrent infections.
  2. May-Hegglin Anomaly (MHA): This rare genetic disorder is characterized by large platelets, which can cause problems with blood clotting.
  3. Bernard-Soulier Syndrome (BSS): This condition affects the adhesive properties of platelets, leading to abnormal bleeding.
  4. Glanzmann Thrombasthenia: This disorder results in a lack of glycoprotein IIb/IIIa, which is necessary for platelet aggregation and clot formation.

Diagnosis and Management:

The diagnosis of congenital and hereditary thrombocytopenia purpura often involves a detailed medical history, physical examination, and blood tests to assess platelet count and function. Genetic testing may also be performed to identify specific gene mutations associated with the condition.

Although there is no specific treatment mentioned in this article, management strategies for individuals with congenital and hereditary thrombocytopenia purpura often involve taking precautions to prevent bleeding and regular monitoring of platelet counts. Additionally, individuals may be advised to avoid certain medications or activities that could increase the risk of bleeding.

In conclusion, congenital and hereditary thrombocytopenia purpura is a rare blood disorder characterized by low platelet count and abnormal bleeding. It is important for individuals with this condition to understand their specific type and work closely with healthcare professionals to manage their symptoms and prevent complications.

Treatment of Congenital and hereditary thrombocytopenia purpura:

Treatment Options for Congenital and Hereditary Thrombocytopenia Purpura

Congenital and hereditary thrombocytopenia purpura (CHTP) is a rare blood disorder characterized by a low platelet count, leading to excessive bleeding and easy bruising. Although there is no cure for CHTP, various treatment options can help manage the symptoms and improve the quality of life for affected indi...

To see full information about treatment please Sign up or Log in