Clinical profile of children with haemophilia at the University Hospital of Brazzaville
Haemophilia is a rare hereditary haemorrhagic disease caused by coagulation factor VIII (haemophilia A) or IX (haemophilia B) deficiency. Very few data exist on this disease in Congo. This survey aims to describe the epidemiological and clinical aspects of the children affected.
| Main Authors: | , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Sciendo
2020-06-01
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| Series: | The Journal of Haemophilia Practice |
| Subjects: | |
| Online Access: | https://doi.org/10.17225/jhp00159 |
| _version_ | 1797832428877774848 |
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| author | Galiba Atipo Tsiba FO Ngolet OL Ngakengni NY Ollandzobo Ikobo LC Nziengui-Mboumba JV Elira Dokekias A |
| author_facet | Galiba Atipo Tsiba FO Ngolet OL Ngakengni NY Ollandzobo Ikobo LC Nziengui-Mboumba JV Elira Dokekias A |
| author_sort | Galiba Atipo Tsiba FO |
| collection | DOAJ |
| description | Haemophilia is a rare hereditary haemorrhagic disease caused by coagulation factor VIII (haemophilia A) or IX (haemophilia B) deficiency. Very few data exist on this disease in Congo. This survey aims to describe the epidemiological and clinical aspects of the children affected. |
| first_indexed | 2024-04-09T14:07:38Z |
| format | Article |
| id | doaj.art-7d8ac2e9356f4a9d84b8dfdc1b4a2445 |
| institution | Directory Open Access Journal |
| issn | 2055-3390 |
| language | English |
| last_indexed | 2024-04-09T14:07:38Z |
| publishDate | 2020-06-01 |
| publisher | Sciendo |
| record_format | Article |
| series | The Journal of Haemophilia Practice |
| spelling | doaj.art-7d8ac2e9356f4a9d84b8dfdc1b4a24452023-05-06T15:59:46ZengSciendoThe Journal of Haemophilia Practice2055-33902020-06-0171535810.17225/jhp00159Clinical profile of children with haemophilia at the University Hospital of BrazzavilleGaliba Atipo Tsiba FO0Ngolet OL1Ngakengni NY2Ollandzobo Ikobo LC3Nziengui-Mboumba JV4Elira Dokekias A5Haematology Department, University Hospital of Brazzaville; Faculty of Health Sciences, Marien Ngouabi University of Brazzaville, Congo.Haematology Department, University Hospital of Brazzaville; Faculty of Health Sciences, Marien Ngouabi University of Brazzaville, CongoPaediatric Department, University Hospital of Brazzaville; Faculty of Health Sciences, Marien Ngouabi University of Brazzaville, CongoPaediatric Department, University Hospital of Brazzaville; Faculty of Health Sciences, Marien Ngouabi University of Brazzaville, CongoHaematology Department, University Hospital of Brazzaville, CongoHaematology Department, University Hospital of Brazzaville; Faculty of Health Sciences, Marien Ngouabi University of Brazzaville, CongoHaemophilia is a rare hereditary haemorrhagic disease caused by coagulation factor VIII (haemophilia A) or IX (haemophilia B) deficiency. Very few data exist on this disease in Congo. This survey aims to describe the epidemiological and clinical aspects of the children affected.https://doi.org/10.17225/jhp00159childrenhaemophiliacircumcisionhaemorrhagearthropathycongo |
| spellingShingle | Galiba Atipo Tsiba FO Ngolet OL Ngakengni NY Ollandzobo Ikobo LC Nziengui-Mboumba JV Elira Dokekias A Clinical profile of children with haemophilia at the University Hospital of Brazzaville The Journal of Haemophilia Practice children haemophilia circumcision haemorrhage arthropathy congo |
| title | Clinical profile of children with haemophilia at the University Hospital of Brazzaville |
| title_full | Clinical profile of children with haemophilia at the University Hospital of Brazzaville |
| title_fullStr | Clinical profile of children with haemophilia at the University Hospital of Brazzaville |
| title_full_unstemmed | Clinical profile of children with haemophilia at the University Hospital of Brazzaville |
| title_short | Clinical profile of children with haemophilia at the University Hospital of Brazzaville |
| title_sort | clinical profile of children with haemophilia at the university hospital of brazzaville |
| topic | children haemophilia circumcision haemorrhage arthropathy congo |
| url | https://doi.org/10.17225/jhp00159 |
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