Medical complications of achondroplasia: a multicentre patient review

被引:178
作者
Hunter, AGW
Bankier, A
Rogers, JG
Sillence, D
Scott, CI
机构
[1] Univ Ottawa, Dept Pediat, Childrens Hosp Eastern Ontario, Dept Genet, Ottawa, ON K1H 8L1, Canada
[2] Royal Childrens Hosp, Dept Genet, Parkville, Vic 3052, Australia
[3] Univ Sydney, Dept Paediat & Child Hlth, New Childrens Hosp, Parramatta, NSW 2124, Australia
[4] Alfred I duPont Hosp Children, Wilmington, DE USA
关键词
achondroplasia; otitis media; tibial bowing; neurological signs;
D O I
10.1136/jmg.35.9.705
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学]; 090102 [作物遗传育种];
摘要
Achondroplasia is the most :prevalent chondrodysplasia and numerous authors have documented the varied social and medical complications that may compromise a full and productive life. Complications include cervicomedullary compression, spinal stenosis, restrictive and obstructive lung disease, otitis media, and tibial bowing, among others. These known complications have led to recommendations for the anticipatory management of such patients. There are relatively few data on the actual rates and timing of these problems. This paper reports data on the rates and age of occurrence of several of these complications based on a review of recorded chart information of 193 patients ascertained from several well established genetic centres with a known interest in the chondrodysplasias. The length of follow up varied and the rates of occurrence at specific age intervals were used to estimate the cumulative percentage affected for each complication. The report includes information on otitis media, ventilation tubes, hearing loss, tonsillectomy, speech problems, tibial bowing and osteotomy, ventricular shunting, apnoea, cervicomedullary decompression, and neurological signs attributable to spinal stenosis.
引用
收藏
页码:705 / 712
页数:8
相关论文
共 37 条
[1]
CRANIOCERVICAL DECOMPRESSION FOR CERVICOMEDULLARY COMPRESSION IN PEDIATRIC-PATIENTS WITH ACHONDROPLASIA [J].
ARYANPUR, J ;
HURKO, O ;
FRANCOMANO, C ;
WANG, H ;
CARSON, B .
JOURNAL OF NEUROSURGERY, 1990, 73 (03) :375-382
[2]
BERKOWITZ R G, 1991, Ear Nose and Throat Journal, V70, P305
[3]
SPINAL-DISORDERS OF DWARFISM - REVIEW OF THE LITERATURE AND REPORT OF 80 CASES [J].
BETHEM, D ;
WINTER, RB ;
LUTTER, L ;
MOE, JH ;
BRADFORD, DS ;
LONSTEIN, JE ;
LANGER, LO .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 1981, 63 (09) :1412-1425
[4]
Cohen M. M., 1976, ORAL FACIAL GENETICS, P523
[5]
NEUROLOGICAL ABNORMALITIES IN ACHONDROPLASTIC CHILDREN [J].
COHEN, ME ;
ROSENTHAL, AD ;
MATSON, DD .
JOURNAL OF PEDIATRICS, 1967, 71 (03) :367-+
[6]
CRAWFORD DB, 1976, 76989 NIH, P301
[7]
DUNBAR JP, 1980, AM J ORTHOD DENTOFAC, V96, P255
[8]
Fortuna A, 1989, J Neurosurg Sci, V33, P185
[9]
FRANCOMANO CA, 1993, AM J HUM GENET S, V53, pA112
[10]
AUDIOLOGICAL FINDINGS OF PATIENTS WITH ACHONDROPLASIA [J].
GLASS, L ;
SHAPIRO, I ;
HODGE, SE ;
BERGSTROM, L ;
RIMOIN, DL .
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 1981, 3 (02) :129-135