Apert syndrome: Diagnostic and management problems in a resource-limited country

Apert syndrome or acrocephalosyndactyly is a rare genetic disease characterized by craniofacial dysmorphism and syndactyly of the hands and feet. We report an observation in a 4-month-old female infant, whose father was 65 years old. The infant was admitted to the neonatology of Sourô Sanou Universi...

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Detalles Bibliográficos
Autores principales: Barro, Makoura, Ouedraogo, Yahaya S., Nacro, Fatimata S., Sanogo, Bintou, Kombasséré, Solange O., Ouermi, Alain S., Tamboura, Hassane, Cessouma, Raymond K., Nacro, Boubacar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Scientific Publications, Pavia, Italy 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6908957/
https://www.ncbi.nlm.nih.gov/pubmed/31871604
http://dx.doi.org/10.4081/pr.2019.8224

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6908957/
https://www.ncbi.nlm.nih.gov/pubmed/31871604
http://dx.doi.org/10.4081/pr.2019.8224

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