Pierre Robin sequence: A series of 117 consecutive cases

被引:106
作者
Holder-Espinasse, M
Abadie, V
Cormier-Daire, V
Beyler, C
Manach, Y
Munnich, A
Lyonnet, S
Couly, G
Amiel, J
机构
[1] Hop Necker Enfants Malad, Dept Genet, F-75743 Paris, France
[2] Hop Necker Enfants Malad, Dept Paediat, F-75743 Paris, France
[3] Hop Necker Enfants Malad, Dept Otorhinolaryngol, F-75743 Paris, France
[4] Hop Necker Enfants Malad, Maxillofacial Surg Unit, F-75743 Paris, France
关键词
D O I
10.1067/mpd.2001.117784
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
A series of 117 cases of Pierre Robin Sequence are classified as isolated (48%), syndromic (35%), and with associated anomalies (17%); the latter group had a poor long-term prognosis. In isolated Pierre Robin Sequence, familial cases and a high incidence of twins were noted. Among syndromic Pierre Robin Sequence, 4 syndromes represent more than 50% of the diagnoses.
引用
收藏
页码:588 / 590
页数:3
相关论文
共 15 条
  • [1] INCIDENCE OF THE ANOMALAD,ROBIN (PIERRE-ROBIN SYNDROME)
    BUSH, PG
    WILLIAMS, AJ
    [J]. BRITISH JOURNAL OF PLASTIC SURGERY, 1983, 36 (04): : 434 - 437
  • [2] THE PIERRE-ROBIN-SEQUENCE - REVIEW OF 125 CASES AND EVOLUTION OF TREATMENT MODALITIES
    CAOUETTELABERGE, L
    BAYET, B
    LAROCQUE, Y
    [J]. PLASTIC AND RECONSTRUCTIVE SURGERY, 1994, 93 (05) : 934 - 942
  • [3] Cohen MM, 1999, AM J MED GENET, V84, P311
  • [4] SYNDROMOLOGYS MESSAGE FOR CRANIOFACIAL BIOLOGY
    COHEN, MM
    [J]. JOURNAL OF MAXILLOFACIAL SURGERY, 1979, 7 (02): : 89 - 109
  • [5] COHEN MM, 1976, J ORAL SURG, V34, P587
  • [6] Elliott Margaret A., 1995, Pediatric Dentistry, V17, P106
  • [7] U-SHAPED PALATAL DEFECT IN ROBIN ANOMALAD - DEVELOPMENTAL AND CLINICAL RELEVANCE
    HANSON, JW
    SMITH, DW
    [J]. JOURNAL OF PEDIATRICS, 1975, 87 (01) : 30 - 33
  • [8] Jones K L., 1997, SMITHS RECOGNIZABLE, P234
  • [9] Recent demographic change in France
    Prioux, F
    [J]. POPULATION, 2000, 55 (03): : 441 - 475
  • [10] Robin P, 1934, AM J DIS CHILD, V48, P541