论文部分内容阅读
先天性双鼻后孔闭锁为一少见疾病,特别是家族中多发者更为罕见。我院先后收治2例,系亲生姐妹。其父母为姨表近亲结婚。 例1 姐,16岁,1984年1月19日入院,住院号;268151。病史:生后双鼻腔完全闭塞,张口呼吸,不能哺乳,在吮乳时曾多次窒息,自幼靠人工喂养。睡觉时打鼾,鼻腔有涕不能(扌省)出,气味香臭不辨,有时头痛。因长期张口呼吸自觉咽干。无耳症状。检查:营养中等,发育正常。说话呈闭塞性鼻音,略呈增殖体面容。牙列不整,硬腭高拱。鼻
Congenital double nasal posterior orifice atresia as a rare disease, especially in the family of multiple are more rare. Our hospital has treated 2 cases, the Department of biological sisters. His parents married aunt cousin. Example 1 Sister, 16 years old, admitted to hospital on January 19, 1984, hospital number; 268151. History: double nasal cavity after birth completely occluded, mouth breathing, can not breast-feeding, sucking milk had multiple asphyxia, since childhood by artificial feeding. Sleeping snoring, nasal mucus can not (扌 Province) out, smell aroma does not distinguish, sometimes headache. Due to long-term mouth breathing conscious throat. No ear symptoms. Check: medium nutrition, normal development. Oral occlusion was nasal tone, a slight proliferation of body surface. Dentition is not full, high palatal arch. nose