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

• Main Authors: Ad Bafa Ibrahim Ouattara (Author), Makoura Barro (Author), Sahoura Fatimata Nacro (Author), Ibraïma Traoré (Author), Bintou Sanogo (Author), Jean W. Diallo (Author), Boubacar Nacro (Author)
• Format: Book
• Published: MDPI AG, 2020-04-01T00:00:00Z.
• Subjects: article
• Online Access: 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...