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
2012 ◽  
Vol 22 (4) ◽  
pp. 444-446
Author(s):  
S. Bamba ◽  
F. Barro-Traoré ◽  
M. Liance ◽  
O. Da ◽  
C. Sanou ◽  
...  

Respiration ◽  
2016 ◽  
Vol 92 (1) ◽  
pp. 1-8 ◽  
Author(s):  
Matthieu Buscot ◽  
Héloïse Pottier ◽  
Charles-Hugo Marquette ◽  
Sylvie Leroy

2018 ◽  
Vol 08 (02) ◽  
pp. 199-206
Author(s):  
A. Kaboré ◽  
A. Diallo ◽  
H. Savadogo ◽  
S. A. P. Ouédraogo ◽  
K. Nagalo ◽  
...  

2019 ◽  
Vol 4 (1) ◽  
pp. 33-36
Author(s):  
Khaly Bane ◽  
Wendpoulomdé AD Kaboré ◽  
Yolande Gnagne-Koffi ◽  
Marie-Chantal Avoaka-Boni ◽  
Anta Seck ◽  
...  

2020 ◽  
Vol 12 (1) ◽  
Author(s):  
Ad Bafa Ibrahim Ouattara ◽  
Makoura Barro ◽  
Sahoura Fatimata Nacro ◽  
Ibraïma Traoré ◽  
Bintou Sanogo ◽  
...  

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.


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