Department of Pediatrics, Division of Metabolic Diseases and Genetics, Erasmus MC University Medical Center-Sophia Children's Hospital, Rotterdam, the Netherlands.
J Inherit Metab Dis. 2010 Oct;33(5):597-602. doi: 10.1007/s10545-010-9144-0. Epub 2010 Jul 2.
Little information is available regarding the auditory function in Pompe patients. Hearing loss has been reported in classic infantile patients, but it is still unknown whether central nervous system involvement interferes with auditory function and whether enzyme replacement therapy can improve hearing. Auditory function has not been studied in children with milder forms of the disease. We analyzed repetitive auditory brainstem response measurements and pure tone audiometry in 24 children with Pompe disease. Only 1 of 13 patients with milder phenotypes showed recurrent conductive hearing loss, while 10 out of 11 classic infantile patients had sensorineural hearing defects. These patients also had a high prevalence of conductive hearing loss. Five patients showed evidence of mild retrocochlear pathology, suggestive of glycogen accumulation in the central nervous system. Hearing loss persisted during therapy in all patients. The results emphasize the need for careful monitoring of auditory function in classic infantile Pompe patients, and for early implementation of hearing aids to protect speech and language development.
有关 Pompe 病患者听觉功能的信息很少。经典婴儿型患者曾有报道听力损失,但中枢神经系统受累是否会影响听觉功能以及酶替代疗法是否能改善听力仍不清楚。对于疾病较轻的患儿,听觉功能尚未进行研究。我们分析了 24 例 Pompe 病患儿的重复听觉脑干反应测量和纯音听阈。仅有 13 例较轻表型的患者出现复发性传导性听力损失,而 11 例经典婴儿型患者则有感觉神经性听力缺陷。这些患者也有较高的传导性听力损失发生率。5 例患者表现出轻度耳蜗后病理学的证据,提示中枢神经系统中糖原积累。所有患者在治疗期间听力损失持续存在。结果强调了在经典婴儿型 Pompe 病患者中需要仔细监测听觉功能,并尽早使用助听器以保护言语和语言发育的必要性。