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

• Main Authors: Makoura Barro (Author), Yahaya S. Ouedraogo (Author), Fatimata S. Nacro (Author), Bintou Sanogo (Author), Solange O. Kombasséré (Author), Alain S. Ouermi (Author), Hassane Tamboura (Author), Raymond K. Cessouma (Author), Boubacar Nacro (Author)
• Format: Book
• Published: MDPI AG, 2019-12-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

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 Univers...