Kpemissi E, Bakonde B, Agbere A, Boko E, Kessie K, Medji L A
Service d'ORL CHU Tokoin Lomé, Togo.
Dakar Med. 1995;40(2):163-6.
The choanal atresia is a rare congenital malformation. Its clinical diagnosis is easy and must be done at the birth by the midwife or the obstetrician. We recommend the aspiration in all hospital maternity wards. This attitude avoids the unrecognized of an unilateral choanal atresia. The authors report three cases with a successfully treatment.
后鼻孔闭锁是一种罕见的先天性畸形。其临床诊断容易，必须在出生时由助产士或产科医生进行。我们建议在所有医院产科病房进行抽吸检查。这种做法可避免单侧后鼻孔闭锁未被识别。作者报告了三例治疗成功的病例。
