Hearing, language, speech, vestibular, and dentofacial disorders in fetal alcohol syndrome

被引:77
作者
Church, MW
Eldis, F
Blakley, BW
Bawle, EV
机构
[1] WAYNE STATE UNIV, SCH MED, DEPT OBSTET & GYNECOL, DETROIT, MI 48201 USA
[2] WAYNE STATE UNIV, SCH MED, DEPT AUDIOL, DETROIT, MI 48201 USA
[3] WAYNE STATE UNIV, SCH MED, DEPT OTOLARYNGOL, DETROIT, MI 48201 USA
[4] CHILDRENS HOSP MICHIGAN, DIV GENET, DETROIT, MI 48201 USA
[5] CHILDRENS HOSP MICHIGAN, MARIE CARLS COMMUN DISORDERS CLIN, DETROIT, MI 48201 USA
关键词
birth defects; craniofacial/dentofacial anomalies; fetal alcohol syndrome (FAS); hearing disorders; language disorders;
D O I
10.1097/00000374-199704000-00008
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
Fetal alcohol syndrome (FAS) is characterized by congenital anomalies traditionally associated with hearing disorders. The present study sought to (a) evaluate possible central hearing loss; (b) verify and extend previous observations on sensorineural and conductive hearing losses; (c) evaluate possible vestibular disorders; (d) examine the relationships between hearing, speech, language, vestibular, and dentofacial disorders in FAS patients; and (e) evaluate the influence of patient age, race, and gender on the expression of these morbidities. A biracial group of 22 FAS patients (aged 3 to 26 years) were evaluated by standard hearing, speech, language, and vestibular tests. Dentofacial and other malformations were also assessed. Of the 22 FAS patients, 17 (77%) had intermittent conductive hearing loss due to recurrent serous otitis media that persisted from early childhood into adulthood, whereas 6 (27%) had sensorineural hearing loss in addition to the conductive hearing loss. Among the 12 patients tested for central hearing function, all (100%) were significantly impaired. Among the patients tested for speech and language ability, 18 of 20 (90%) had speech pathology, 16 of 21 (76%) had expressive language deficits, and 18 of 22 (82%) had receptive language deficits. Hearing, speech, and language deficits were not influenced by age, race, or gender. On the vestibular tests, all performed within normal limits with the possible exception of one child (n = 6). High incidences of dentofacial, temporomandibular joint, ocular, cardiac, and skeletal disorders were observed. Race and gender tended to influence dental malocclusion class. Two subjects exhibited autistic tendencies. In conclusion, new and important findings included a high prevalence of sensorineural, conductive, and central hearing deficits, the persistence of otitis proneness into adulthood, the existence of temporomandibular joint disorders, and the possible influence of gender or race on dental malocclusions. Such disorders can contribute to the learning, behavioral, and emotional difficulties seen in FAS patients and warrant early, aggressive intervention.
引用
收藏
页码:227 / 237
页数:11
相关论文
共 73 条
[21]   EFFECTS OF PRENATAL ALCOHOL EXPOSURE AT SCHOOL AGE .1. PHYSICAL AND COGNITIVE-DEVELOPMENT [J].
COLES, CD ;
BROWN, RT ;
SMITH, IE ;
PLATZMAN, KA ;
ERICKSON, S ;
FALEK, A .
NEUROTOXICOLOGY AND TERATOLOGY, 1991, 13 (04) :357-367
[22]   COMPREHENSIVE TREATMENT OF CHILDREN WITH RECURRENT SEROUS OTITIS-MEDIA [J].
DOWNS, MP ;
JAFEK, B ;
WOOD, RP .
OTOLARYNGOLOGY-HEAD AND NECK SURGERY, 1981, 89 (04) :658-665
[23]  
DOWNS MP, 1980, SEMIN SPEECH LANG HE, V1, P25
[24]   A CEPHALOMETRIC ASSESSMENT OF CHILDREN WITH FETAL ALCOHOL SYNDROME [J].
GIR, AV ;
AKSHARANUGRAHA, K ;
HARRIS, EF .
AMERICAN JOURNAL OF ORTHODONTICS AND DENTOFACIAL ORTHOPEDICS, 1989, 95 (04) :319-326
[25]   INCREASED METABOLISM OF ACETAMINOPHEN IN CHRONICALLY ALCOHOLIC PATIENTS [J].
GIRRE, C ;
HISPARD, E ;
PALOMBO, S ;
NGUYEN, C ;
DALLY, S .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1993, 17 (01) :170-173
[26]   A LONG RANGE EVALUATION OF CLEFT PALATE REPAIR [J].
GLOVER, DM .
PLASTIC AND RECONSTRUCTIVE SURGERY, 1961, 27 (01) :19-&
[27]  
GRAHAM M D, 1963, Trans Am Acad Ophthalmol Otolaryngol, V67, P213
[28]  
HANNIGAN JH, 1995, ALCOHOLISM CLIN EX S, V19, pA53
[29]  
HOLBROW CA, 1966, J LARYNGOSCOPE, V76, P762
[30]  
HOLM VA, 1969, PEDIATRICS, V43, P833