Pediatric Hematology Center, Synphaet Children’s Hospital

Care for all pediatric blood disorders: Early diagnosis increases treatment success.

Pale complexion, fatigue, weakness, easy bruising, pin-point bleeding spots, frequent nosebleeds, or a palpable abdominal mass—these signs should not be overlooked. They are warning signs of “Pediatric Blood Disorders,” which are caused by abnormalities of red blood cells, white blood cells, platelets, or the blood clotting system. Many blood disorders can be screened, diagnosed, and treated early to prevent severe complications, helping your child return to good health and grow normally.

Synphaet Children’s Hospital is ready to stand by every family with our Pediatric Hematology Center. We provide comprehensive screening, diagnosis, and treatment for pediatric hematological disorders by a team of expert pediatric hematologists, utilizing precise medical technology and standardized laboratories to give parents peace of mind at every step of care.

Conditions Treated at the Pediatric Hematology Center

We diagnose, treat, and manage hematological disorders in children from newborns to adolescents.

• Anemia: Thalassemia and hemoglobinopathies, G6PD deficiency, iron deficiency anemia, vitamin deficiency anemia, anemia of chronic disease, and hemolytic anemia.
• Platelet and Coagulation Disorders: Hemophilia, Immune Thrombocytopenia (ITP), and other clotting factor deficiencies.
• Hematologic Malignancies: Leukemia, lymphoma, and certain bone marrow disorders.
• Other Hematological Abnormalities: Leukopenia (low white blood cell count causing susceptibility to infections), erythrocytosis (high red blood cell count), thrombocytosis (high platelet count), lymphadenopathy (enlarged lymph nodes), hepatomegaly, and splenomegaly (enlarged liver or spleen).

Diagnostic Services and Specialized Treatments

• Hematology Laboratory Testing: Complete Blood Count (CBC), hemoglobin typing (Hb Typing), iron profiles, coagulation factor assays, G6PD enzyme level tests, and other genetic blood disorder screenings.
• Bone Marrow Aspiration & Biopsy: Performed by specialists to accurately diagnose leukemia and aplastic anemia.
• Treatment and Therapeutic Care: Medical management with antivirals/antibiotics, safe blood and blood component transfusions, iron replacement therapy, and long-term care plans.

Why choose the Pediatric Hematology Center at Synphaet Children’s Hospital?

• ✓ Expert Pediatric Hematology Team: Treatment plans are personalized and managed by highly experienced pediatric hematologists.
• ✓ High-Standard Laboratories and Blood Components: Fast and accurate blood analysis, paired with a safe screening and matching system for pediatric blood transfusions.
• ✓ Multidisciplinary Team: Seamless coordination with other pediatric specialists, nurses, nutritionists, and allied health professionals for holistic care.
• ✓ Compassionate Care and Family Counseling: Deep guidance on diet, daily activities, preventing injuries in children prone to bleeding, and family planning for genetic blood disorders.

Frequently Asked Questions (Q&A)

Q: How can I tell if my child is becoming pale or anemic?

A: Parents can observe if the inner lower eyelids, lips, palms, soles of the feet, or fingernails look paler than usual. This may be accompanied by tiredness, lack of energy, reduced milk intake, or sleepiness. If these symptoms occur, a blood test should be done to evaluate red blood cell concentration.

Q: Is it dangerous if my child bruises easily or gets frequent nosebleeds?

A: If your child bruises easily without significant impact, has pin-point red bleeding spots on the skin, or gets nosebleeds that are hard to stop even after applying pressure for a long time, it could indicate thrombocytopenia (low platelets) or a clotting disorder. You should take your child to see a doctor for immediate coagulation testing.

Q: Are all childhood blood disorders hereditary?

A: No, they are not. While some blood disorders are genetic, such as thalassemia, many others are caused by nutritional deficiencies, autoimmune issues, infections, or other non-genetic causes. A detailed diagnosis is necessary to find the cause.

Q: Can thalassemia in children be permanently cured?

A: Thalassemia is a genetic disorder. Currently, the main treatment involves appropriate blood transfusions, iron chelation therapy, and general healthcare to reduce complications. However, a permanent cure is possible through blood stem cell or bone marrow transplantation, which the physician will evaluate on a case-by-case basis.

Q: Can children with blood disorders live a normal life?

A: Most children can attend school, play, and live a life close to normal if they receive proper treatment and follow-up care as recommended by their physician.