Prenatal sonographic diagnosis of skeletal dysplasias. A report of 47 cases

被引:71
作者
Doray, B
Favre, R
Viville, B
Langer, B
Dreyfus, M
Stoll, C
机构
[1] Hop Hautepierre, Serv Genet Med, F-67098 Strasbourg, France
[2] CMCO, Serv Echog Gynecol & Obstet, Strasbourg, France
[3] Hop Civil, Strasbourg, France
[4] Hop Hautepierre, Serv Gynecol 2, F-67098 Strasbourg, France
[5] Hop Hautepierre, Serv Gynecol 1, F-67098 Strasbourg, France
来源
ANNALES DE GENETIQUE | 2000年 / 43卷 / 3-4期
关键词
achondroplasia; osteochondrodysplasias; osteogenesis imperfects; prenatal diagnosis; screening; ultrasound;
D O I
10.1016/S0003-3995(00)01026-1
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The purpose of this study was to evaluate the foetal sonographic efficiency for prenatal diagnosis of osteochondrodysplasias. Forty-seven prenatal and postnatal cases diagnosed between January 1993 and December 1998 in the referral sonographic centres of Strasbourg were studied. All cases were reviewed retrospectively and the prenatal ultrasound findings and diagnosis were compared to the postnatal or post-mortem diagnosis. Each case was studied by ultrasonographers, geneticists, radiologists, and foetopathologists. Final diagnosis was based on clinical examination, skeletal survey and molecular testing as deemed necessary. Routine screening and dating was the indication for foetal sonography in 72 % (32/47) of our cases. The most likely time of diagnosis was between 16 and 24 weeks of gestation (17 out of 47 cases, 36 %), which corresponds to the time of foetal anomaly sonographic scan in France. The other cluster of cases (12 among 47, 26 %) was disclosed before 16 weeks of gestation. These results illustrate the importance of a detailed evaluation of the limbs during sonographic examinations of first and second trimesters of pregnancy. While the identification of skeletal dysplasias was relatively easy in our study, the ability to make an accurate specific antenatal diagnosis was more difficult. An accurate diagnosis was proposed in 28 of the 47 cases (60 %). In 19 % of the cases (9/47), the prenatal diagnosis was not accurate; in 21 % of the cases (10/47), the prenatal diagnosis was imprecise. In 45 of the 47 cases (96 %) prenatal foetal scan correctly predicted the prognosis. (C) 2000 Editions scientifiques et medicales Elsevier SAS.
引用
收藏
页码:163 / 169
页数:7
相关论文
共 20 条
  • [1] ANDERSEN PE, 1987, J MED GENET, V27, P37
  • [2] INTERNATIONAL CLASSIFICATION OF OSTEOCHONDRODYSPLASIAS
    BEIGHTON, P
    GIEDION, A
    GORLIN, R
    HALL, J
    HORTON, B
    KOZLOWSKI, K
    LACHMAN, R
    LANGER, LO
    MAROTEAUX, P
    POZNANSKI, A
    RIMOIN, DL
    SILLENCE, D
    SPRANGER, J
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1992, 44 (02): : 223 - 229
  • [3] Camera G, 1982, Prog Clin Biol Res, V104, P441
  • [4] ULTRASOUND EVALUATION OF AMNIOTIC-FLUID VOLUME .2. THE RELATIONSHIP OF INCREASED AMNIOTIC-FLUID VOLUME TO PERINATAL OUTCOME
    CHAMBERLAIN, PF
    MANNING, FA
    MORRISON, I
    HARMAN, CR
    LANGE, IR
    [J]. AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1984, 150 (03) : 250 - 254
  • [5] CHAN AKJ, 1998, AM J HUM GENET S, V63, pA160
  • [6] BONE DYSPLASIAS - THE PRENATAL DIAGNOSTIC CHALLENGE
    ESCOBAR, LF
    BIXLER, D
    WEAVER, DD
    PADILLA, LM
    GOLICHOWSKI, A
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1990, 36 (04): : 488 - 494
  • [7] Gaffney G, 1998, PRENATAL DIAG, V18, P357, DOI 10.1002/(SICI)1097-0223(199804)18:4<357::AID-PD276>3.0.CO
  • [8] 2-0
  • [9] JEANTY P, 1984, J ULTRAS MED, V3, P75
  • [10] Maroteaux P, 1995, MALADIES OSSEUSES EN