scholarly journals Direct Coronal Restoration with Composite Resins: An Assessment of 44 Cases Performed by Students at Yalgado Ouédraogo University Hospital Center of Ouagadougou, Burkina Faso

2019 ◽  
Vol 4 (1) ◽  
pp. 33-36
Author(s):  
Khaly Bane ◽  
Wendpoulomdé AD Kaboré ◽  
Yolande Gnagne-Koffi ◽  
Marie-Chantal Avoaka-Boni ◽  
Anta Seck ◽  
...  
Keyword(s):  
Burkina Faso ◽  
Composite Resins ◽  
University Hospital ◽  
Hospital Center

Mansonelliasis identified by a cervicovaginal smear at the university hospital center of Bobo-Dioulasso (Burkina Faso)

2012 ◽  
Vol 22 (4) ◽  
pp. 444-446
Author(s):  
S. Bamba ◽  
F. Barro-Traoré ◽  
M. Liance ◽  
O. Da ◽  
C. Sanou ◽  
...  
Keyword(s):  
Burkina Faso ◽  
University Hospital ◽  
Bobo Dioulasso ◽  
The University ◽  
Hospital Center

scholarly journals Febrile Convulsions in Infants at the Pediatrics University Hospital Center Charles de Gaulle of Ouagadougou (Burkina Faso)

2018 ◽  
Vol 08 (02) ◽  
pp. 199-206
Author(s):  
A. Kaboré ◽  
A. Diallo ◽  
H. Savadogo ◽  
S. A. P. Ouédraogo ◽  
K. Nagalo ◽  
...  
Keyword(s):  
Burkina Faso ◽  
University Hospital ◽  
Febrile Convulsions ◽  
Charles De Gaulle ◽  
De Gaulle ◽  
Hospital Center

scholarly journals The Seckel syndrome: A case observed in the pediatric department of the University Hospital Center Sourou Sanou (Burkina Faso)

2020 ◽  
Vol 12 (1) ◽  
Author(s):  
Ad Bafa Ibrahim Ouattara ◽  
Makoura Barro ◽  
Sahoura Fatimata Nacro ◽  
Ibraïma Traoré ◽  
Bintou Sanogo ◽  
...  
Keyword(s):  
Burkina Faso ◽  
Female Child ◽  
Mendelian Inheritance ◽  
University Hospital ◽  
Facial Dysmorphism ◽  
Pediatric Department ◽  
Seckel Syndrome ◽  
The University ◽  
Hospital Center

Seckel syndrome-1 or “bird-headed dwarfism”, Online Mendelian Inheritance in Man number 210600, is a rare genetic disease with an autosomal recessive transmission. We report a female child of 56 months diagnosed with SCKL1 at the Pediatric department of the University Hospital Center Sourou Sanou, Burkina Faso. She showed the typical features including facial dysmorphism, dwarfism, microcephalus and mental retardation. Ophthalmic and dental anomaly and extremities were associated. Without a codified etiological treatment, a psychotherapist support, a genetic counseling, a regular pediatric follow-up, a quarterly odontostomatological and ophthalmological follow- up have been recommended.

scholarly journals Epidemiology of Urological Emergencies at the Regional University Hospital Center of Ouahigouya, Burkina Faso

2020 ◽  
Vol 10 (06) ◽  
pp. 177-183
Author(s):  
Mamadou Tiéoulé Traore ◽  
Clôtaire Alexis Marie Kiemdiba Donega Yameogo ◽  
Moussa Kabore ◽  
Souleymane Ouedraogo
Keyword(s):  
Burkina Faso ◽  
University Hospital ◽  
Regional University ◽  
Urological Emergencies ◽  
Hospital Center
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