A 37-year-old Nigerian woman with Apert syndrome – medical and psychosocial perspectives: a case report

BACKGROUND: Apert syndrome is a rare genetic disease that presents a diagnostic dilemma because of its similarity with other craniosynostosis syndromes. Currently, there is paucity of reports about adult patients in African medical literature. Therefore, this case report highlights medical and psych...

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Detalles Bibliográficos
Autores principales: Kana, M. A., Baduku, T. S., Bello-Manga, H., Baduku, A. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5949149/
https://www.ncbi.nlm.nih.gov/pubmed/29753329
http://dx.doi.org/10.1186/s13256-018-1638-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5949149/
https://www.ncbi.nlm.nih.gov/pubmed/29753329
http://dx.doi.org/10.1186/s13256-018-1638-7

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