Stem cell therapy is one of the most promising branches in the medical field, offering potential treatment avenues for a myriad of diseases and conditions. From neurodegenerative disorders to autoimmune diseases, stem cells offer the possibility of regenerating damaged or lost tissue and potentially reversing the course of these conditions. In the near future, it could remedy heart problems, metabolic issues and specific cancers. As its potential is continually being researched and discovered, stem cells are offering hope to countless individuals seeking alternative approaches to managing and, in some cases, treating their health conditions.
Potentially Treatable Diseases With Stem Cell
Acute Leukaemias
Acute Biphenotypic Leukaemia
Acute Lymphocytic Leukaemia (ALL)
Acute Myelogenous Leukaemia (AML)
Acute Lymphoblastic Leukaemia
Acute Undifferentiated Leukaemia
Chronic Leukaemias
Chronic Lymphocytic Leukaemia (CLL)
Chronic Myelogenous Leukaemia (CML)
Juvenile Chronic Myelogenous Leukaemia (JCML)
Juvenile Myelomonocytic Leukaemia (JMML)
Juvenile Myelogenous Leukaemia
Myelodysplastic Syndromes
Amyloidosis
Chronic Myelomonocytic Leukaemia (CMML)
Refractory Anaemia (RA)
Refractory Anaemia with Excess Blasts (RAEB)
Refractory Anaemia with Excess Blasts in Transformation (RAEB-T)
Refractory Anaemia with Ringed Sideroblasts (RARS)
Myeloproliferative Disorders
Acute Myelofibrosis
Agnogenic Myeloid Metaplasia (Myelofibrosis)
Essential Thrombocythaemia
Polycythaemia Vera
Lymphoproliferative Disorders
Hodgkin’s Disease
Non-Hodgkin’s Lymphoma
Prolymphocytic Leukaemia
Inherited Metabolic Disorders
Adrenoleukodystrophy
Alpha Mannosidosis
Beta-Glucuronidase Deficiency (MPS-VII)
Gaucher’s Disease
Hunter’s Syndrome (MPS-Il)
Hurler’s Syndrome (MPS-IH)
Krabbe Disease
Maroteaux-Lamy Syndrome (MPS-VI)
Metachromatic Leukodystrophy
Morquio Syndrome (MPS-IV)
Mucolipidosis Il (I-cell Disease)
Mucopolysaccharidoses (MPS)
Niemann-Pick Disease
Sanfilippo Syndrome (MPS-Ill)
Scheie Syndrome (MPS-lS)
Sly Syndrome
Wolman Disease
Inherited Platelet Abnormalities
Amegakaryocytosis / Congenital Thrombocytopenia
Inherited Erythrocyte Abnormalities
Beta Thalassaemia Major
Blackfan-Diamond Anaemia
Pure Red Cell Aplasia
Sickle Cell Disease
Phagocyte Disorders
Chediak-Higashi Syndrome
Chronic Granulomatous Disease
Neutrophil Actin Deficiency
Reticular Dysgenesis
Histiocytic Disorders
Familial Erythrophagocytic Lymphohistiocytosis
Haemophagocytosis
Histiocytosis X
Langerhans’ Cell Histiocytosis
Congenital (Inherited) Immune System Disorders
Absence of T&B Cells SCID
Absence of T Cells
Normal B Cell SCID
Ataxia-Telangiectasia
Bare Lymphocyte Syndrome
Common Variable Immunodeficiency
DiGeorge Syndrome
Kostmann Syndrome
Leukocyte Adhesion Deficiency
Omenn’s Syndrome
Severe Combined Immunodeficiency (SCID)
SCID with Adenosine Deaminase Deficiency
Wiskott-Aldrich Syndrome
X-Linked Lymphoproliferative Disorder
Stem Cell Disorders
Aplastic Anaemia (Severe)
Congenital Cytopenia
Dyskeratosis Congenita
Fanconi Anaemia
Paroxysmal Nocturnal Hemoglobinuria (PNH)
Plasma Cell Disorders
Multiple Myeloma
Plasma Cell Leukaemia
Waldenstrom’s Macroglobulinaemia
Other Inherited Disorders
Cartilage-Hair Hypoplasia
Ceroid Lipofuscinosis
Congenital Erythropoietic Porphyria
Glanzmann Thrombasthenia
Lesch-Nyhan Syndrome
Osteopetrosis
Tay Sachs Disease
Emerging Treatments
Diabetes
Cerebral Palsy
Brain Injury
Heart Diseases
Stroke