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 Printable version |
La drépanocytose
Sickle-cell anaemia
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Robert Girot, Pierre Bégué, Frédéric Galacteros
2003
Series : Hors collection
Find out the books of Hors collection
ISBN : 2-7420- 0465-3
322 pages
Specialty : Hematology
Published in : French
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Sickle-cell anaemia is a hereditary disease of the haemoglobin. In France it has become one of the main genetic diseases in terms of the number of people affected.
It is a rheological and vascular illness which combines chronic anaemia with various complications. Patients' lives are punctuated by painful crises and a variety of symptoms that often lead them to hospital emergency departments.
In the past 20 years much progress has been made both in treating the main complications of the illness (pain, acute anaemia, serious infections, acute chest syndrome, strokes, etc.) and in preventing them, thus improving patients' longevity and quality of life.
This book sets out to provide the latest information about sickle-cell anaemia, along with the clinical experience of teams working in various medical specialities such as paedriatrics, haematology, internal medicine, genetics, surgery, obstetrics and neurology.
Au sommaire :
- Génétique et physiopathologie de la drépanocytose
- Diagnostic biologique des syndromes drépanocytaires
- Vers de nouvelles thérapeutiques spécifiques de la drépanocytose
- La crise drépanocytaire chez l’enfant
- Traitement de la douleur des crises vaso-occlusives de l’enfant drépanocytaire
- Stratégie de prise en charge des crises vaso-occlusives non compliquées de l’adulte drépanocytaire
- Traitement de la douleur chez l’adulte
- L’anémie chez l’enfant drépanocytaire
- Infections chez l’enfant drépanocytaire
- L’infection chez l’adulte drépanocytaire
- Le syndrome thoracique aigu chez l’enfant
- Syndrome thoracique aigu de l’adulte
- Complications neurologiques et vasculopathie cérébrale au cours de la drépanocytose
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