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pro vyhledávání: '"Fatimata Sahoura Nacro"'
Autor:
Boubacar Nacro, Fatimata Sahoura Nacro, Alain Saga Ouermi, Hassane Tamboura, Bintou Sanogo, Raymond K. Cessouma, Solange O. Kombasséré, Yahaya S. Ouedraogo, Makoura Barro
Publikováno v:
Pediatric Reports, Vol 11, Iss 4 (2019)
Pediatric Reports
Volume 11
Issue 4
Pediatric Reports
Volume 11
Issue 4
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 a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2afd3ca6136bd97003d7e72b4b7690fa
https://www.pagepress.org/journals/index.php/pr/article/view/8224
https://www.pagepress.org/journals/index.php/pr/article/view/8224
