Abstract |
Since 1968, bone marrow transplantation became the first line therapy for selected metabolic and immunological hereditary disorders. Actually, advances in the supportive care in bone marrow transplantation and a better knowledge of the immunology of BMT complications has been associated with a better disease correction and an increase in long term survival. New approaches are under investigation and include: hematopoietic growth factors, enzymatic replacement and gene therapy. However at the present time BMT is still the only curative treatment for selected hereditary disorders.
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Authors | W Bujan, A Ferster, C Devalck, E Vamos, F Mascart, R Denis, N Azzi, P Vergauwen, E Sariban |
Journal | Revue medicale de Bruxelles
(Rev Med Brux)
Vol. 13
Issue 6
Pg. 207-11
(Jun 1992)
ISSN: 0035-3639 [Print] Belgium |
Vernacular Title | La greffe de moelle dans les maladies héréditaires. |
PMID | 1631420
(Publication Type: English Abstract, Journal Article)
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Chemical References |
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Topics |
- Bone Marrow Transplantation
- Chediak-Higashi Syndrome
(therapy)
- Genetic Diseases, Inborn
(classification, therapy)
- Growth Substances
(therapeutic use)
- Humans
- Metabolism, Inborn Errors
(therapy)
- Wiskott-Aldrich Syndrome
(therapy)
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