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 Afric...
https://ift.tt/2rFAxjc
Κυριακή 13 Μαΐου 2018
A 37-year-old Nigerian woman with Apert syndrome – medical and psychosocial perspectives: a case report
Εγγραφή σε:
Σχόλια ανάρτησης (Atom)
Δεν υπάρχουν σχόλια:
Δημοσίευση σχολίου