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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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 owners of this website hereby guarantee to respect the legal confidentiality conditions, applicable in France, and not to disclose this data to third parties.
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The age between years was represented by You may thus request that your data, should it be inaccurate, incomplete, unclear, outdated, not be used or stored, be corrected, clarified, updated or deleted. Personal information regarding our website’s visitors, including their identity, is confidential. Hemoglobinopathy ; Sickle cell anemia homozygoote Anemia ; Africa.
As per the Law relating to information storage and personal integrity, you have the right to oppose art 26 of that lawaccess art 34 of that law and rectify art drepancytose of that law your personal data. Top of the page – Article Outline. The purpose of this study was to determine morbidity, mortality and socioprofessional insertion of homozygous sickle cell patients, followed up in Dakar university hospital.
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Etude de l’hйmogramme dans la drйpanocytose homozygote: а propos de 87 patients
Five patients died during a mean follow-up of 5 years. Men were slightly predominant with a sex-ratio of 1. Homozygous sickle cell disease in patients above 20 years of age: The presence of complications was not significantly influenced by patient’s sex.
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Clinic and paraclinical data, as information in socioprofessional insertion were noted in medical records for analysis. Ongoing challenge are to manage complication and social living for these patients.
All patients had a quarterly hematological check-up and a annual statement to detect chronic complications.