目的探讨突发性耳聋（突聋）与血液流变学和甲襞微循环的改变的关系。
Objective To explore the relationship of the changes of hemorheology and nailfold microcirculation with sudden deafness (SD).
随着分子遗传学技术在致聋基因的克隆、鉴定等方面应用的进展，使得为某些家庭进行遗传咨询成为可能。
Recent advances within molecular genetics to identify the genes for deafness mean that it is now possible for genetic counseling services to offer genetic testing for deafness to certain families.
结论GJB2突变是导致学语前聋的主要原因，28.6%的学语前隐性和18.9%学语前散发非综合征性耳聋病人携带了两个GJB2突变。
Conclusion the mutations in GJB2 are the major cause of prelingual deafness; two causative mutations can be found in (28.6%) prelingual recessive and in (18.9%) prelingual sporadic NSHL patients.
聋儿康复是一门集耳科学、听力学、电声学、心理学、言语病理学、教育学等多学科知识为一体的交叉学科。
Deaf childrens s rehabilitation are subjects accumulation of the otology, audiology, electroacoustics, psychics, speech pathology and education.
结论血液流变学及甲襞微循环的改变可能与突聋的发生相关。
Objective To explore the relationship of the changes of hemorheology and nailfold microcirculation with sudden deafness (SD).
结论血液流变学及甲襞微循环的改变可能与突聋的发生相关。
Objective To explore the relationship of the changes of hemorheology and nailfold microcirculation with sudden deafness (SD).
应用推荐