DREPANOCYTOSE HOMOZYGOTE PDF
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.
|Published (Last):||22 July 2017|
|PDF File Size:||6.23 Mb|
|ePub File Size:||7.53 Mb|
|Price:||Free* [*Free Regsitration Required]|
Access to the full text of this article requires a subscription.
You can move this window by clicking on the headline. Access to the PDF text. The purpose of this study was to determine morbidity, mortality and socioprofessional insertion of homozygous sickle cell patients, followed up in Dakar university hospital. If you are a subscriber, please sign in ‘My Account’ at the top right of the screen.
Contact Help Who are we? Journal page Archives Contents list.
Clinic and paraclinical data, as information in socioprofessional insertion were noted in medical depanocytose for analysis. You may thus request that your data, should it be inaccurate, incomplete, unclear, outdated, not be used or stored, be corrected, clarified, updated or deleted.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.
The age between years was represented by Ongoing challenge are to manage complication and social living for these 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. Men were slightly predominant with a sex-ratio of 1. 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 homozygotr art 36 of that law your personal data.
There was a problem providing the content you requested
Homozygous sickle cell disease in patients above 20 years of age: Hemoglobinopathy ; Sickle cell anemia ; Anemia ; Africa. All patients had a quarterly hematological check-up and a annual statement to detect chronic complications. The presence of complications was not significantly influenced by patient’s sex.
Outline Masquer le plan. Access to the text HTML. Five patients died during a mean follow-up of 5 years.
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. Top of the page – Article Outline. If you want to subscribe to this journal, see our rates You can purchase this item in Pay Per View: