Zobrazeno 1 - 2
of 2
pro vyhledávání: '"T S, Baduku"'
Publikováno v:
Journal of Medical Case Reports, Vol 12, Iss 1, Pp 1-5 (2018)
Abstract 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
Externí odkaz:
https://doaj.org/article/5d8bd6e150794610afe064f67df41809
Autor:
T S, Baduku
Publikováno v:
Nigerian journal of clinical practice. 24(7)
There has been a slow but steady decline in the frequency of contrast fluoroscopic studies performed all over the world, including oesophagography. This trend is attributed to the increasing availability of endoscopy, computed tomography (CT), and ma