Hone Stephen W, Smith Richard J H
Department of Pediatric Otolaryngology/HNS, University of Iowa Hospitals and Clinics, 21201 PFP, 200 Hawkins Drive, Iowa City, IA 52242, USA.
Otolaryngol Clin North Am. 2002 Aug;35(4):751-64. doi: 10.1016/s0030-6665(02)00048-8.
Specific investigations of pediatric hearing loss are based on the history, physical examination, and age of the patient. The radiographic investigation of choice is high-resolution CT of the temporal bone. Patients with a dilated vestibular aqueduct need to be investigated further for Pendred syndrome. Screening for mutations in connexin 26 has become increasingly available in many centers and should be performed in all cases of nonsyndromic hearing loss. It is important to understand the implications and pitfalls of genetic testing. Genetic counseling is necessary.
小儿听力损失的具体检查基于患者的病史、体格检查和年龄。首选的影像学检查是颞骨高分辨率CT。前庭导水管扩张的患者需要进一步检查是否患有彭德莱综合征。在许多中心,连接蛋白26突变的筛查越来越普遍,所有非综合征性听力损失病例均应进行此项检查。了解基因检测的意义和陷阱很重要。基因咨询是必要的。