Prenatal Diagnosis of Fetal Cataract: Case Report and Review of the Literature

被引:13
作者
Leonard, Alexandre [1 ]
Bernard, Pierre [1 ]
Hiel, Anne-Lise [1 ]
Hubinont, Corinne [1 ]
机构
[1] Catholic Univ Louvain, St Luc Univ Hosp, Dept Obstet, BE-1200 Brussels, Belgium
关键词
Fetal; Ultrasound; Eye; Lens; Cataract; Congenital abnormalities; Aneuploidy; RHIZOMELIC CHONDRODYSPLASIA PUNCTATA; HALLERMANN-STREIFF-SYNDROME; NANCE-HORAN-SYNDROME; CONGENITAL CATARACT; ULTRASONOGRAPHIC DIAGNOSIS; BILATERAL CATARACT; TURNER-SYNDROME; APERT-SYNDROME; EYE; MICROPHTHALMIA;
D O I
10.1159/000238117
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objectives: To report a case of prenatally diagnosed fetal cataract and conduct a systematic review of previously reported cases. Methods: Review of the literature based mainly on Pubmed search using specific keywords in order to list cataract causes diagnosed prenatally and in early childhood, isolated or associated with microphthalmia. Results and Discussion: A differential diagnosis list and specific prenatal diagnosis testing are suggested in order to offer the best management of this rare fetal condition. Copyright (C) 2009 S. Karger AG, Basel
引用
收藏
页码:61 / 67
页数:7
相关论文
共 72 条
  • [41] ORZALESI N, 1981, ARCH OPHTHALMOL-CHIC, V99, P69
  • [42] Prenatal diagnosis of the Cerebro-Oculo-Facio-Skeletal (COFS) syndrome
    Paladini, D
    D'Armiento, M
    Ardovino, I
    Martinelli, P
    [J]. ULTRASOUND IN OBSTETRICS & GYNECOLOGY, 2000, 16 (01) : 91 - 93
  • [43] Panda A, 1981, Indian J Ophthalmol, V29, P377
  • [44] Prenatal diagnosis of Turner syndrome -: Report on 69 cases
    Papp, Csaba
    Beke, Artur
    Mezei, Gabor
    Szigeti, Zsanett
    Ban, Zoltan
    Papp, Zoltan
    [J]. JOURNAL OF ULTRASOUND IN MEDICINE, 2006, 25 (06) : 711 - 717
  • [45] Fetal cataract in congenital toxoplasmosis
    Pedreira, DAL
    Diniz, EMA
    Schultz, R
    Faro, LB
    Zugaib, M
    [J]. ULTRASOUND IN OBSTETRICS & GYNECOLOGY, 1999, 13 (04) : 266 - 267
  • [46] Human microphthalmia associated with mutations in the retinal homeobox gene CHX10
    Percin, EF
    Ploder, LA
    Yu, JJ
    Arici, K
    Horsford, DJ
    Rutherford, A
    Bapat, B
    Cox, DW
    Duncan, AMV
    Kalnins, VI
    Kocak-Altintas, A
    Sowden, JC
    Traboulsi, E
    Sarfarazi, M
    McInnes, RR
    [J]. NATURE GENETICS, 2000, 25 (04) : 397 - 401
  • [47] Puder K S, 1997, Infect Dis Obstet Gynecol, V5, P262, DOI 10.1155/S1064744997000446
  • [48] Rahi JS, 2000, INVEST OPHTH VIS SCI, V41, P2108
  • [49] Prenatal detection of congenital bilateral cataract leading to the diagnosis of Nance-Horan syndrome in the extended family
    Reches, Adi
    Yaron, Yuval
    Burdon, Kathryn
    Crystal-Shalit, Ornit
    Kidron, Dvora
    Malcov, Mira
    Tepper, Ron
    [J]. PRENATAL DIAGNOSIS, 2007, 27 (07) : 662 - 664
  • [50] Clinicopathological study of bilateral developmental cataracts diagnosed in utero
    Roberts, F
    Wisdom, S
    Howatson, AG
    Imrie, S
    [J]. GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, 2006, 244 (02) : 237 - 242