Congenital bowing of long bones: Prenatal ultrasound findings and diagnostic dilemmas

被引:9
作者
Farra, C [1 ]
Piquet, C [1 ]
Guillaume, M [1 ]
D'Ercole, C [1 ]
Philip, N [1 ]
机构
[1] Assistance Publ Hop Marseille, Hop Enfants La Timone, Dept Genet Med, Ctr Diagnost Prenatal, Marseille, France
关键词
prenatal diagnosis; bowing of the long bones; kyphomelic clysplasia; campomelic dysplasia; Stuve-Wiedemann syndrome;
D O I
10.1159/000059376
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: Bowing of the long bones can be easily detected on antenatal ultrasound screening, but it is a nonspecific sign that can be associated with a variety of conditions, each denoting a different prognosis. Among these conditions, three well-differentiated bone dysplasias share bowed long bones as a main clinical manifestation. Campomelic dysplasia and Stuve-Wiedemann syndrome are characterized by a poor prognosis. Conversely, the overall prognosis of children affected with kyphomelic dysplasia is good, the intelligence and motor development are normal and the radiological abnormalities tend to improve and regress with age. Case Report. We report a case of prenatal detection of short and bowed femora at the 22nd week of gestation. Careful US examination as well as in utero X-ray of the skeleton allowed the exclusion of campomelic dysplasia. In the absence of an unambiguous diagnosis, the pregnancy was continued. At birth, the child presented with clinical and radiological features consistent with a diagnosis of kyphomelic dysplasia. Conclusion: This case illustrates the difficulties in making an accurate diagnosis and consequently giving a prognosis when isolated femoral bowing is found on fetal ultrasound examination. Copyright (C) 2002 S. Karger AG, Basel.
引用
收藏
页码:236 / 239
页数:4
相关论文
共 16 条
[1]   Kyphomelic dysplasia in two sib fetuses [J].
Chen, CP ;
Chern, SR ;
Shih, SL ;
Chuang, CY ;
Huang, FY .
JOURNAL OF MEDICAL GENETICS, 1998, 35 (01) :65-69
[2]   Variability in kyphomelic dysplasia [J].
Cisarik, F ;
Kozlowski, K ;
Masel, J ;
Sillence, D .
PEDIATRIC RADIOLOGY, 1999, 29 (07) :551-557
[3]   ASSOCIATION OF KYPHOMELIC DYSPLASIA WITH SEVERE COMBINED IMMUNODEFICIENCY [J].
CORDER, WT ;
HUMMEL, M ;
MILLER, C ;
WILSON, NW .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1995, 57 (04) :626-629
[4]  
Cormier-Daire V, 1998, AM J MED GENET, V78, P146, DOI 10.1002/(SICI)1096-8628(19980630)78:2<146::AID-AJMG9>3.0.CO
[5]  
2-M
[6]   CAMPOMELIC DYSPLASIA AND AUTOSOMAL SEX REVERSAL CAUSED BY MUTATIONS IN AN SRY-RELATED GENE [J].
FOSTER, JW ;
DOMINGUEZSTEGLICH, MA ;
GUIOLI, S ;
KWOK, C ;
WELLER, PA ;
STEVANOVIC, M ;
WEISSENBACH, J ;
MANSOUR, S ;
YOUNG, ID ;
GOODFELLOW, PN ;
BROOK, JD ;
SCHAFER, AJ .
NATURE, 1994, 372 (6506) :525-530
[7]  
KHAVAJI A, 1976, PEDIATR RADIOL, V120, P641
[8]  
Kozlowski K, 1996, AM J MED GENET, V63, P17
[9]   SKELETAL DYSPLASIA WITH SHORT, ANGULATED FEMORA (KYPHOMELIC DYSPLASIA) [J].
MACLEAN, RN ;
PRATER, WK ;
LOZZIO, CB .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1983, 14 (02) :373-380
[10]   A CLINICAL AND GENETIC-STUDY OF CAMPOMELIC DYSPLASIA [J].
MANSOUR, S ;
HALL, CM ;
PEMBREY, ME ;
YOUNG, ID .
JOURNAL OF MEDICAL GENETICS, 1995, 32 (06) :415-420