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

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, B...

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Detalles Bibliográficos
Autores principales: Ouattara, Ad Bafa Ibrahim, Barro, Makoura, Nacro, Sahoura Fatimata, Traoré, Ibraïma, Sanogo, Bintou, Diallo, Jean W., Nacro, Boubacar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Scientific Publications, Pavia, Italy 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7160856/
https://www.ncbi.nlm.nih.gov/pubmed/32308969
http://dx.doi.org/10.4081/pr.2020.8231

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7160856/
https://www.ncbi.nlm.nih.gov/pubmed/32308969
http://dx.doi.org/10.4081/pr.2020.8231

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