Dr Rahul Bhargava

MBBS, MD, DM (Clinical Haematology)

Principal Director & Chief Hematology at Fortis Hospital

MBBS, MD, DM (Clinical Haematology)

Principal Director & Chief Hematology at Fortis Hospital

Bernard-Soulier Syndrome

Contact Us

Related Videos :

Frequently Asked Questions (FAQ) :

No, Bernard-Soulier Syndrome is not curable, but symptoms can be managed effectively through treatments like platelet transfusions and antifibrinolytic medications.

 

Yes, BSS is inherited in an autosomal recessive pattern, so both parents must carry the defective gene for a child to inherit the condition.

 

With proper management and medical care, most patients with BSS can lead relatively normal lives, though they must take precautions to avoid injuries and manage bleeding.

 

About Bernard-Soulier Syndrome

Bernard-Soulier Syndrome (BSS) is a rare genetic blood disorder that affects platelet function. Platelets are cells responsible for blood clotting, and in BSS, these platelets are abnormally large and fewer in number. This condition often leads to excessive bruising, prolonged bleeding after injury, and sometimes spontaneous bleeding. The syndrome is inherited in an autosomal recessive pattern, meaning both parents must carry the defective gene for a child to be affected.

Causes of Bernard-Soulier Syndrome

The primary cause of Bernard-Soulier Syndrome is a mutation in the genes that control glycoproteins in platelets, specifically the GP1BA, GP1BB, or GP9 genes. These glycoproteins play a vital role in platelet adhesion, which is crucial for clot formation. Without normal functioning of these glycoproteins, the platelets cannot properly adhere to the blood vessel walls, resulting in bleeding issues.

Types of Bernard-Soulier Syndrome

Bernard-Soulier Syndrome can be classified based on the type of genetic mutation:

  1. Classic Bernard-Soulier Syndrome: Characterized by large platelets and a significant reduction in platelet count.
  2. Variant Forms: Includes cases where specific glycoproteins are affected differently, leading to variations in severity and symptoms.

Symptoms of Bernard-Soulier Syndrome

The symptoms of Bernard-Soulier Syndrome often manifest early in life, typically during childhood. Common symptoms include:

  • Easy bruising
  • Excessive bleeding after cuts or surgeries
  • Frequent nosebleeds
  • Heavy menstrual periods in women
  • Bleeding gums
  • Petechiae (tiny red or purple spots caused by bleeding under the skin)

In severe cases, individuals may experience spontaneous bleeding without any obvious cause.

Diagnosis of Bernard-Soulier Syndrome

Diagnosing Bernard-Soulier Syndrome involves a combination of clinical examination, family history, and specialized blood tests. Dr. Rahul Bhargava recommends the following diagnostic approaches:

  • Complete Blood Count (CBC): To check for low platelet counts and large platelets.
  • Platelet Aggregation Tests: To assess the functionality of platelets.
  • Flow Cytometry: A technique used to analyze the glycoproteins on the surface of platelets.
  • Genetic Testing: To confirm mutations in the GP1BA, GP1BB, or GP9 genes.

Early and accurate diagnosis is crucial for managing the symptoms and preventing complications.

Treatment of Bernard-Soulier Syndrome

While there is no definitive cure for Bernard-Soulier Syndrome, the treatment focuses on managing symptoms and preventing excessive bleeding. Dr. Rahul Bhargava recommends the following treatment strategies:

  1. Platelet Transfusions: In severe cases of bleeding or during surgery, platelet transfusions can be administered to replenish the platelet count.
  2. Antifibrinolytic Agents: Medications like tranexamic acid help reduce bleeding, especially during dental procedures or surgeries.
  3. Avoidance of Certain Medications: Patients with BSS should avoid aspirin and nonsteroidal anti-inflammatory drugs (NSAIDs), as these can worsen bleeding.
  4. Iron Supplements: In cases of chronic bleeding, iron supplementation may be required to prevent anemia.

Cost of Treatment and Stay in India

Lorem ipsum dolor sit amet, consectetur adipiscing elit. Ut elit tellus, luctus nec ullamcorper mattis, pulvinar dapibus leo.

×