Literature DB >> 17390522

[Haematological and biochemical outline of patients with sickle cell disease SS and SC in steady state in the National Hospital Center Yalgado Ouedraogo of Ouagadougou].

E W C Nacoulma, J Sakande, E Kafando, E D Kpowbié, I P Guissou.   

Abstract

Burkina Faso belongs to the sicklemic's belt of LEHMAN and is the epicenter of haemoglobin C. This is the reason of this study on the haematological and biochemical parameters of homozygotes SS and double heterozygotes SC in stationary stage. These parameters will be use for comparison during crisis and to evaluate the therapy efficiency. So 20 homozygotes and 20 double heterozygotes were studied. The blood film showed anaemia with an haemoglobin rate average of 7.8 g/dl for SS against 9.8 g/dl for SC (p < 0.001). An serum's iron elevated in 26.3% of the SS with an average of 23 micromoles /l against 36.8% with an average of 21.7 micromoles /l in the SC (p < 0.001). These results show the importance of SS anaemia's and biochemical's disorders in comparison to the SC.

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Year:  2006        PMID: 17390522

Source DB:  PubMed          Journal:  Mali Med        ISSN: 0464-7874


  6 in total

1.  [Sickle cell disease in stationary phase in 6-59 months children in Lubumbashi: epidemiology and clinical features].

Authors:  Mick Ya Pongombo Shongo; Olivier Mukuku; Toni Kasole Lubala; Augustin Mulangu Mutombo; Gray Wakamb Kanteng; Winnie Sombodi Umumbu; Robert Mbuli Lukamba; Stanislas Okitotsho Wembonyama; Oscar Numbi Luboya
Journal:  Pan Afr Med J       Date:  2014-09-24

2.  [Evaluation of hemogram in patients with homozygous sickle cell disease: about 87 cases].

Authors:  Fatima Dahmani; Souad Benkirane; Jaafar Kouzih; Aziz Woumki; Hassan Mamad; Azlarab Masrar
Journal:  Pan Afr Med J       Date:  2016-12-20

3.  Clinical profile of sickle cell disease in children treated at "Cliniques Universitaires de Bukavu" and "Clinique Ami des Enfants", Bukavu, Democratic Republic of the Congo.

Authors:  Viviane Feza Bianga; Mwanza Nangunia; Fernand Manga Oponjo; John Mambo Itongwa; Judicaël Iragi Mushubusha; Moise Mbaluku Colombe; Carmel Mbalo Walemba; Okitosho Wembonyama
Journal:  Pan Afr Med J       Date:  2022-02-03

4.  [Hematological and nutritional profile of homozygous sickle cell SS aged 6 to 59 months in Lubumbashi, Democratic Republic of Congo].

Authors:  Mick Ya Pongombo Shongo; Olivier Mukuku; Augustin Mulangu Mutombo; Toni Kasole Lubala; Paul Makinko Ilunga; Winnie Umumbu Sombodi; Stanislas Okitotsho Wembonyama; OscarNumbi Luboya
Journal:  Pan Afr Med J       Date:  2015-08-11

5.  [Epidemiological profile of hemoglobinopathies: a cross-sectional and descriptive index case study].

Authors:  Fatima Dahmani; Souad Benkirane; Jaafar Kouzih; Aziz Woumki; Hassan Mamad; Azlarab Masrar
Journal:  Pan Afr Med J       Date:  2017-06-29

6.  [Epidemiological, clinical and hematological profiles of homozygous sickle cell disease during the intercritical period among children in Ziguinchor, Senegal].

Authors:  Lamine Thiam; Assane Dramé; Isabelle Zokébé Coly; François Niokhor Diouf; Ndiogou Seck; Djibril Boiro; Aliou Abdoulaye Ndongo; Idrissa Basse; Babacar Niang; Indou Deme/Ly; Assane Sylla; Ibrahima Diagne; Ousmane Ndiaye
Journal:  Pan Afr Med J       Date:  2017-11-07
  6 in total

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