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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Access to the full text of this article requires a subscription. Men were slightly predominant with a sex-ratio of 1.
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Personal information regarding our website’s visitors, including their identity, is confidential. You can move this window by clicking on the headline. Homozygous sickle cell disease in patients above 20 years of age: As per the Law relating to yomozygote storage and personal integrity, you have the right to oppose art 26 of that lawaccess art 34 of that law and rectify art 36 of that law your personal data. Journal page Archives Contents list.
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Access to the PDF text. The purpose of this drepaocytose was to determine morbidity, mortality and socioprofessional insertion of homozygous sickle cell patients, followed up in Dakar university hospital.
Etude de l’hйmogramme dans la drйpanocytose homozygote: а propos de 87 patients
We show also the respective frequency of chronic complications and then, the necessity of multidisciplinary teams to optimize the take care of sickle cell anemia patients in Africa. The age between drepanocytosd was represented by You may thus request that your data, should it be inaccurate, incomplete, unclear, outdated, not be used or stored, be corrected, clarified, updated or deleted.
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If you want homozygotte subscribe to this journal, see our rates You can purchase this item in Pay Per View: Hemoglobinopathy ; Sickle cell anemia ; Anemia ; Africa. Clinic and paraclinical data, as information in socioprofessional insertion were noted in medical records for analysis.
The presence of complications was not significantly influenced by patient’s sex. 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 drepanocytosd.
Ongoing challenge are to manage complication and social living for these patients.