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

• প্রধান লেখক: Ad Bafa Ibrahim Ouattara (লেখক), Makoura Barro (লেখক), Sahoura Fatimata Nacro (লেখক), Ibraïma Traoré (লেখক), Bintou Sanogo (লেখক), Jean W. Diallo (লেখক), Boubacar Nacro (লেখক)
• বিন্যাস: গ্রন্থ
• প্রকাশিত: MDPI AG, 2020-04-01T00:00:00Z.
• বিষয়গুলি: article
• অনলাইন ব্যবহার করুন: Connect to this object online.

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 Souro...