Admiraal R J, Huygen P L
Department of Otorhinolaryngology, University Hospital Nijmegen, P.O. Box 9101, 6500 HB, Nijmegen, The Netherlands.
Int J Pediatr Otorhinolaryngol. 2000 Sep 29;55(2):133-42. doi: 10.1016/s0165-5876(00)00395-5.
An aetiological study was performed on 57 pupils at the deaf-blind department of the Institute for the Deaf at Sint-Michielsgestel, The Netherlands, in the school year 1998-1999 and on 49 deaf-blind pupils at the same department in the school year 1986-1987. The pupils were 5-20 years of age. In addition, the aetiologies were studied in 55 deaf infant pupils in 1998 and compared with those of 68 deaf infant pupils in 1988. Their age was 1-5 years. All the pupils showed hearing impairment with thresholds of >60 dB HL. Among the deaf-blind pupils and deaf infant pupils, there were several cases with rare hereditary syndromes. The prevalence of acquired causes of deafness, especially congenital rubella, had decreased over the years, whereas perinatal causes of deafness had increased. Chromosomal anomalies were found in 15% of the infant pupils in 1998. Over the study period, the percentage of pupils with multiple handicaps increased from 25 to 38%.
1998 - 1999学年,对荷兰辛特 - 米歇尔斯盖斯特尔聋人研究所聋盲部的57名学生进行了病因学研究,并于1986 - 1987学年对该部门的49名聋盲学生进行了病因学研究。这些学生年龄在5至20岁之间。此外,1998年对55名失聪婴儿学生的病因进行了研究,并与1988年的68名失聪婴儿学生的病因进行了比较。他们的年龄在1至5岁之间。所有学生均表现出听力障碍,听力阈值>60 dB HL。在聋盲学生和失聪婴儿学生中,有几例患有罕见的遗传综合征。多年来,后天性耳聋病因的患病率,尤其是先天性风疹,有所下降,而围产期耳聋病因有所增加。1998年,15%的婴儿学生被发现存在染色体异常。在研究期间,多重残疾学生的比例从25%增加到了38%。