scholarly journals Maternal Mortality in the Gynecology-Obstetric Department at the Yalgado Ouedraogo University Hospital Center (CHUYO), Burkina Faso: About 181 Cases Collected from January 1<sup>st</sup> to December 31<sup>st</sup> 2016

2020 ◽  
Vol 10 (05) ◽  
pp. 714-722
Author(s):  
Sibraogo Kiemtoré ◽  
Komboigo Béwendin Evelyne ◽  
Simporé André ◽  
Zamané Hyacinthe ◽  
Kaboré Xavier ◽  
...  
2012 ◽  
Vol 22 (4) ◽  
pp. 444-446
Author(s):  
S. Bamba ◽  
F. Barro-Traoré ◽  
M. Liance ◽  
O. Da ◽  
C. Sanou ◽  
...  

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

2021 ◽  
Vol 11 (08) ◽  
pp. 1026-1036
Author(s):  
Salifou Badariatou ◽  
Atadé Sèdjro Raoul ◽  
Sidi Imorou Rachidi ◽  
Obossou Achille Awede ◽  
Sounouvi Ernest ◽  
...  

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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