Why Cord Blood Banking is Important?

  • India has the largest number of children with thalassemia major in the world, about 1 to 1.5 lakh, and about 10,000-15,000 children having thalassemia major are born every year.

  • After the USA and China, India ranks 3rd highest in reported cases of Blood Cancer.

  • There are nearly 25,000 children diagnosed with cancer in India every year and around 9000 of these have leukemia.

TREATMENT AVAILABLE FOR
SPECTRUM OF DISEASES

There are more than 80 Conditions approved for treatment with Cord Blood Stem Cells!

  • Acute Biphenotypic Leukemia
  • Acute Lymphoblastic Leukemia (ALL)
  • Acute Myelofibrosis
  • Acute Myelogenous Leukemia (AML)
  • Acute Undifferentiated Leukemia
  • Agnogenic Myeloid Metaplasia
  • Aplastic Anemia
  • Beta Thalassemia Major
  • Chronic Lymphocytic Leukemia (CLL)
  • Chronic Myelogenous Leukemia (CML)
  • Chronic Myelomonocytic Leukemia (CMML)
  • Congenital Dyserythropoietic Anemia
  • Congenital Thrombocytopenia
  • Diamond-Blackfan Anemia
  • Essential Thrombocythemi
  • Fanconi Anemia
  • Glanzmann Thrombasthenia
  • Hodgkin’s Lymphoma
  • Juvenile Chronic Myelogenous Leukemia (JCML)
  • Juvenile Myelomonocytic Leukemia (JMML)
  • Medulloblastoma
  • Neuroblastoma
  • Non-Hodgkin’s Lymphoma (Burkitt’s Lymphoma)
  • Paroxysmal Nocturnal Hemoglobinuria (PNH)
  • Plasma Cell Leukemia
  • Polycythemia Vera
  • Pure Red Cell Aplasia
  • Refractory Anemia
  • Refractory Anemia with Excess Blasts
  • Refractory Anemia with Excess Blasts in Transformation
  • Retinoblastoma
  • Shwachman-Diamond Syndrome
  • Sideroblastic Anemia
  • Sickle Cell Disease
  • Waldenstrom’s Macroglobulinemia
  • Adrenoleukodystrophy (ALD)
  • Hunter Syndrome (MPS-II)
  • Hurler Syndrome (MPS-IH)
  • Krabbe Disease
  • Lesch-Nyhan Syndrome
  • Maroteaux-Lamy Syndrome (MPS-VI)
  • Metachromatic Leukodystrophy
  • Morquio Syndrome (MPS-IV)
  • Mucolipidosis II (I-cell Disease)
  • Niemann-Pick Disease
  • Osteopetrosis
  • Pelizaeus-Merzbacher Disease
  • Sandhoff Disease
  • Sanfilippo Syndrome (MPS-III)
  • Scheie Syndrome (MPS-IS)
  • Sly Syndrome (MPS-VII)
  • Wolman Disease
  • Ataxia-Telangiectasia
  • Bare Lymphocyte Syndrome
  • Cartilage-Hair Hypoplasia
  • Chediak-Higashi Syndrome
  • Chronic Granulomatous Disease (CGD)
  • Common Variable Immunodeficiency
  • DiGeorge Syndrome
  • Erythropoietic Porphyria
  • Hemophagocytic Lymphohistiocytosis
  • Hermansky-Pudlak Syndrome
  • Kostmann Syndrome
  • Leukocyte Adhesion Deficiency
  • Lymphoproliferative Disorders, X-linked
  • Multiple Myeloma
  • Myelokathexis
  • Neutrophil Actin Deficiency
  • Omenn Syndrome
  • Pearson’s Syndrome
  • Reticular Dysgenesis
  • SCID which is X-linked
  • SCID with absence of T & B Cells
  • SCID with absence of T Cells, Normal B Cells
  • SCID with Adenosine Deaminase Deficiency
  • Systemic Mastocytosis
  • Wiskott-Aldrich Syndrome
  • Acute Biphenotypic Leukemia
  • Acute Lymphoblastic Leukemia (ALL)
  • Acute Myelofibrosis
  • Acute Myelogenous Leukemia (AML)
  • Acute Undifferentiated Leukemia
  • Agnogenic Myeloid Metaplasia
  • Aplastic Anemia
  • Beta Thalassemia Major
  • Chronic Lymphocytic Leukemia (CLL)
  • Chronic Myelogenous Leukemia (CML)
  • Chronic Myelomonocytic Leukemia (CMML)
  • Congenital Dyserythropoietic Anemia
  • Congenital Thrombocytopenia
  • Diamond-Blackfan Anemia
  • Essential Thrombocythemi
  • Fanconi Anemia
  • Glanzmann Thrombasthenia
  • Hodgkin’s Lymphoma
  • Juvenile Chronic Myelogenous Leukemia (JCML)
  • Juvenile Myelomonocytic Leukemia (JMML)
  • Medulloblastoma
  • Neuroblastoma
  • Non-Hodgkin’s Lymphoma (Burkitt’s Lymphoma)
  • Paroxysmal Nocturnal Hemoglobinuria (PNH)
  • Plasma Cell Leukemia
  • Polycythemia Vera
  • Pure Red Cell Aplasia
  • Refractory Anemia
  • Refractory Anemia with Excess Blasts
  • Refractory Anemia with Excess Blasts in Transformation
  • Retinoblastoma
  • Shwachman-Diamond Syndrome
  • Sideroblastic Anemia
  • Sickle Cell Disease
  • Waldenstrom’s Macroglobulinemia
  • Adrenoleukodystrophy (ALD)
  • Hunter Syndrome (MPS-II)
  • Hurler Syndrome (MPS-IH)
  • Krabbe Disease
  • Lesch-Nyhan Syndrome
  • Maroteaux-Lamy Syndrome (MPS-VI)
  • Metachromatic Leukodystrophy
  • Morquio Syndrome (MPS-IV)
  • Mucolipidosis II (I-cell Disease)
  • Niemann-Pick Disease
  • Osteopetrosis
  • Pelizaeus-Merzbacher Disease
  • Sandhoff Disease
  • Sanfilippo Syndrome (MPS-III)
  • Scheie Syndrome (MPS-IS)
  • Sly Syndrome (MPS-VII)
  • Wolman Disease
  • Ataxia-Telangiectasia
  • Bare Lymphocyte Syndrome
  • Cartilage-Hair Hypoplasia
  • Chediak-Higashi Syndrome
  • Chronic Granulomatous Disease (CGD)
  • Common Variable Immunodeficiency
  • DiGeorge Syndrome
  • Erythropoietic Porphyria
  • Hemophagocytic Lymphohistiocytosis
  • Hermansky-Pudlak Syndrome
  • Kostmann Syndrome
  • Leukocyte Adhesion Deficiency
  • Lymphoproliferative Disorders, X-linked
  • Multiple Myeloma
  • Myelokathexis
  • Neutrophil Actin Deficiency
  • Omenn Syndrome
  • Pearson’s Syndrome
  • Reticular Dysgenesis
  • SCID which is X-linked
  • SCID with absence of T & B Cells
  • SCID with absence of T Cells, Normal B Cells
  • SCID with Adenosine Deaminase Deficiency
  • Systemic Mastocytosis
  • Wiskott-Aldrich Syndrome