- Red Blood Cells - which transport oxygen
- White Blood Cells - which produce antibodies and fight bacteria
- Platelets - which assist blood clotting
- A guaranteed match for autologous transplants (where the donor and recipient are the same individual)
- A readily available supply of stored HSCs. This compares well to having to do a national or international search which is costly and time-consuming in an already time critical situation.
- Lower risk of Graft vs. Host Disease for autologous transplants, a situation where the transplanted tissue attacks the patients own tissue.
- Ease of collection, which is pain-free and risk-free to both mother and child.
- UCB stem cells are more vigorous, have a higher rate of engraftment and are more tolerant to tissue mismatches, compared to other types of stem cells, e.g. bone marrow.
Malignant diseases (cancers):
- Acute Lymphocytic Leukemia
- Acute Myelocytic Leukemia
- Acute Promyelocytic Leukemia
- Chronic Myelogeneous Leukemia
- Juvenile Chronic Myelogeneous Leukemia
- Juvenile Mono-Myelocytic Leukemia
- Myeloid/Natural Killer (NK) Cell Precursor Acute Leukemia
- Myelodysplastic syndromes
- Refractory anemia
- Refractory anemia with ringed sideroblasts
- Refractory anemia with excess blasts
- Refractory anemia with excess blasts in transformation
- Chronic myelomonocytic leukemia
- Neuroblastoma
- Polymphocytic Leukemia
- Agnogenic myeloid metaplasia (also called Myelofibrosis)
- Amegakaryocytic Thrombocytopenia
- Blackfan-Diamond Syndrome
- Cerebral X-linked Adrenoleukodystrophy (ALD)
- Dyskeratosis Congenita
- Evans syndrome
- Familial Erythrophagocytic Lymphohistiocytosis
- Fanconi’s Anemia
- Globoid Cell Leukodystrophy (also called Krabbe disease)
- Gunther Disease
- Hurler Syndrome
- Kostmann Syndrome
- Lesch Nyhan Syndrome
- Maroteaux-Lamy Syndrome
- Osteopetrosis
- Paroxysmal Nocturnal Hemoglobinuria
- Pure Red Cell Aplasia
- Purine Nucleotide Phosphorylase Deficiency
- Reticular Dysgenesis
- Severe Aplastic Anemia
- Severe Combined Immune Deficiency (SCID)
- SCID with absence of T & B cells
- SCID with absence of T cells, normal B cells
- Combined Immmunodeficiency
- Common Variable Immunodeficiency
- Sickle Cell Anemia
- Thalassemia (Major)
- Thymic Dysplasia
- Wiskott-Aldrich Syndrome
- X-linked Lymphoproliferative Syndrome
- X-linked HyperIgM syndrome
- Lymphomas:
- Burkitt’s Lymphoma
- Hodgkin’s Disease
- Non-Hodgkin’s Lymphoma
- Multiple Myeloma
- (Alpha-)Mannosidosis
- Aspartylglycoasminuria
- Bare Lymphocyte Syndrome
- Chediak-Higashi Syndrome
- Chronic Granulomatous Disease
- Congenital Neutropenia
- DiGeorge Syndrome
- Histiocytosis X (also called Langerhans’ Cell Histiocytosis)
- Hurler-Scheie Syndrome
- Gangliosidosis
- Glanzmann's Thrombasthenia
- Omenn Syndrome
- Leukocyte Adhesion Deficiency
- Mucolipidosis II (I cell disease)
- Metachromatic leukodystrophy
- Neuronal/Infantile Ceroid Lipofuscinosis (also called Batten Disease)
- Nezelof Syndrome
- Sialidosis
- Shwachman–Diamond syndrome
- Sly Syndrome
- Tay-Sachs Syndrome
- Wolman Disease
Malignant diseases:
- Acute Biphenotypic Leukemia*
- Acute Undifferentiated Leukemia*
- Mantle Cell Lymphoma
- Brain tumour*
- Ewing Sarcoma*
- Ovarian Cancer*
- Renal Cell Carcinoma*
- Rhabdomyosarcoma
- Small Cell Lung Cancer*
- Testicular Cancer*
- Rescue after autologous bone marrow transplant failure
- Systemic Lupus Erythematosus
- Amyloidosis
- Congenital Amegakaryocytic Thrombocytopenia
- Congenital Cytopenia*
- Congenital Dyserythropoietic Anemia
- Griscelli Syndrome
- Idiopathic Thrombocytopenic Purpura
- Polycythemia Vera*
- Fucosidosis
- Gaucher’s Disease*
- Niemann-Pick Disease*
- Sandhoff Disease*
- SCID with Adenosine Deaminase Deficiency*
- Thrombocytopenia
- Nijmegen Breakage Syndrome
- Chronic Active Epstein Barr (resulting in lymphoproliferative disease)
- X-linked Immune Dysregulation Polyendocrine Enteropathy
- Multiple Sclerosis *
- Rheumatoid Arthritis*
- Type 1 Diabetes*
- Cerebral palsy*
- Raetz et al., BMT, 1997
- Shaw et al., Pediatric Transplantation, 1999
- S. J. Fasouliotis, J.G. Schenker / European Journal of Obstetrics & Gynecology and Reproductive Biology, 2000
- Ballen et al., BBMT, 2001
- Gluckman et al., Exp Hematol., 2004
- Martin et al., BBMT, 2004
- Gluckman and Wagner, BMT, 2008
- www.marrow.org
- www.cordblood.com
- www.nationalcordbloodprogram.org
Last update 4th Aug 2011.
![]() | Saving our first-born's cord blood stem cells was a no-brainer for my husband and me. As new parents we want to be able to provide the best options we can for Noah; we'd also like to try and start preparing for his future. Cord blood banking does both for us. We don't know if or when we'll be needing the stored cord blood stem cells, but it gives us a sense of security and peace that, should we ever need it, the best solutions are available to us. We chose CordLife for 2 reasons – their service quality and the fact that they have a facility in Manila. It just made a lot more sense to us and we're so happy we did it! | ![]() |
Gillian Akiko Thomson-Guevara 3-time Olympian, gold medalist SEA Games and entrepreneur |
Type 1 diabetes
A clinical trial underway at the University of Florida is examining how an infusion of autologous cord blood stem cells into children with Type 1 diabetes will impact metabolic control over time, as compared to standard insulin treatments. Preliminary results demonstrate that an infusion of cord blood stem cells is safe and may provide some slowing of the loss of insulin production in children with type 1 diabetes![]() | Cord blood banking was a completely new concept to me when I had my first child, but I had read up on it due to the fact that my mom was diagnosed with stage 3b cancer the year prior to my pregnancy – and I wanted to do my tiny part in perhaps saving a family member’s life down the line. With percentages high on potentially saving lives within my family – I knew that I wanted to do this for those I love more than life itself. | ![]() |
Lexi Schulze Berenguer-Testa TV Host and Magazine Editor |






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