La drépanocytose homozygote, fait partie des hémoglobinopathies les plus fréquentes au Maroc. La drépanocytose est caractérisée par une grande variabilité. La revue de médecine interne – Vol. 24 – N° 11 – p. – La drépanocytose homozygote après l’âge de 20 ans: suivi d’une cohorte de patients au CHU . Request PDF on ResearchGate | Lithiase biliaire et drépanocytose homozygote en pédiatrie à Dakar (Sénégal) | Background Cholelithiasis is a well recognized.
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Etude de l’hйmogramme dans la drйpanocytose homozygote: а propos de 87 patients
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Access to the text HTML. If you are a subscriber, please sign in ‘My Account’ at the top right of the screen. Access to the full text of this article requires a subscription. The presence of complications was not significantly influenced by patient’s sex.
Cahiers d’études et de recherches francophones / Santé
Homozygous sickle cell disease in patients above 20 years of age: The purpose of this study was to determine morbidity, mortality and socioprofessional insertion of homozygous sickle cell patients, followed up in Dakar university hospital. Journal page Archives Contents list. You may thus request that your data, should it be inaccurate, incomplete, unclear, outdated, not be used or stored, be corrected, clarified, dfepanocytose or deleted.
The age between years was represented by The owners of this website hereby guarantee to respect the legal confidentiality conditions, applicable in France, and not to disclose this data to third parties. If you want to subscribe to this journal, see our rates You can purchase this item in Pay Per View: Outline Masquer le plan. Ongoing challenge are to manage complication and social living for these patients.
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All patients had a quarterly hematological check-up and a annual statement to detect chronic complications. Five patients died during a mean follow-up of 5 years.
Men were slightly predominant with a sex-ratio of 1. Top of the page – Article Outline. Hemoglobinopathy ; Sickle cell anemia ; Anemia ; Africa.
You can move this window by clicking on the headline. We show also the homozygotd frequency of chronic complications and then, the necessity of multidisciplinary teams to optimize the take care of sickle cell anemia patients in Africa.
Clinic and paraclinical data, as information in socioprofessional insertion were noted in medical records for analysis. Contact Help Who are we?