遗传性耳聋可分为两种:一种为综合征性耳聋(syndromic hearing impairment,SHI),另一种为非综合征性耳聋(non-syndromic hearing impairment,NSHI...
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遗传性耳聋可分为综合征性耳聋(syndromic hearing loss,SHL)和非综合征性耳聋(nonsyndromic hearing loss,NSHL)。目前与遗传性 .
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遗传性耳聋可分为综合征性耳聋(syndromic hearing loss,SHL)和非综合征性耳聋(nonsyndromic hearing loss,NSHL)。目前与遗传性 .
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非综合征性耳聋 nonsyndromic hearing impairment ; Nonsyndromic hearing loss ; NSHL
分为综合征性耳聋 syndromic hearing impairment ; syndromic hearing loss ; SHI
和非综合征性耳聋 nonsyndromic hearing loss ; nonsyndromic hearing impairment ; NSHL
为非综合征性耳聋 nonsyndromic hearing impairment ; NSHI
可以分为综合征性耳聋 syndromic hearing impairment ; SHI
分为非综合征性耳聋 nonsyndromic hearing impairment
称为非综合征性耳聋 nonsyndromic hearing impairment
目的探讨母系遗传性非综合征性耳聋的听力学特征及分子遗传学机制。
Objective To explore audiological features of matrilineal non syndromic deafness and its molecular mechanism.
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.
名为Alport综合征的遗传性肾炎。病人通常表现为神经性耳聋及眼病。
This is a type of hereditary nephritis known as Alport's syndrome in which patients may also manifest nerve deafness and eye problems.
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