First Trimester Fetal Clubfoot: A Novel Presentation of Severe Osteogenesis Imperfecta

被引:0
|
作者
Barnett, Chloe [1 ]
Eddy, Kaitlyn [2 ]
Rauk, Phillip N. [3 ]
Lewter, Jill [2 ]
机构
[1] Allina Hlth Minnesota Perinatal Phys, Minneapolis, MN 55404 USA
[2] M Hlth Fairview Maternal Fetal Med, Minneapolis, MN USA
[3] Univ Minnesota, Dept Obstet Gynecol & Womens Hlth, Med Sch, Minneapolis, MN USA
关键词
clubfoot; fetal fractures; first trimester ultrasound; osteogenesis imperfecta; skeletal dysplasia; talipes equinovarus; PRENATAL-DIAGNOSIS; I PROCOLLAGEN; LETHAL; COLLAGEN; MUTATIONS; GENETICS; GENES;
D O I
10.1002/ajmg.a.63867
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Talipes equinovarus, also called clubfoot, is a relatively common congenital defect affecting approximately one in every 1000 live births. Most cases of clubfoot are expected to be idiopathic and unrelated to an underlying genetic syndrome. In approximately 20% of cases, a clear genetic etiology is identified. Here we present two cases of bilateral clubfoot identified via fetal ultrasound in the first trimester associated with osteogenesis imperfecta diagnosed in the second trimester. Both fetuses presented with multiple fractures and were identified to have loss-of-function variants in COL1A1. An association between clubfeet in the first trimester and osteogenesis imperfecta has not been previously reported to the best of our knowledge, which leads to unique opportunities for prompt diagnosis, genetic counseling and testing, and appropriate management.
引用
收藏
页数:5
相关论文
共 50 条
  • [31] OSTEOGENESIS IMPERFECTA - REVIEW OF LITERATURE WITH PRESENTATION OF 29 CASES
    SHOENFELD, Y
    FRIED, A
    EHRENFELD, NE
    [J]. AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1975, 129 (06): : 679 - 687
  • [32] Intrapartum fetal pain management in lethal osteogenesis imperfecta
    McCarthy, Elizabeth A.
    Watkins, Andrew
    Shub, Alexis
    Walker, Susan P.
    [J]. PRENATAL DIAGNOSIS, 2012, 32 (10) : 1013 - 1015
  • [33] DIAGNOSIS AND MANAGEMENT OF FETAL OSTEOGENESIS IMPERFECTA CONGENITA IN LABOR
    ZERVOUDAKIS, IA
    STRONGIN, MJ
    SCHROTENBOER, KA
    BEHAN, M
    KAZAM, E
    HAWKS, GG
    [J]. AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1978, 131 (01) : 116 - 117
  • [34] Osteogenesis imperfecta type 2: A fetal case report
    不详
    [J]. VIRCHOWS ARCHIV, 2005, 447 (02) : 277 - 278
  • [35] A Novel Biallelic Splice Site Variant in the SPARC Gene Causing Severe Osteogenesis Imperfecta
    Agnes Selina
    Deeptiman James
    Vrisha Madhuri
    [J]. Indian Journal of Pediatrics, 2023, 90 : 626 - 626
  • [36] A Novel Biallelic Splice Site Variant in the SPARC Gene Causing Severe Osteogenesis Imperfecta
    Selina, Agnes
    James, Deeptiman
    Madhuri, Vrisha
    [J]. INDIAN JOURNAL OF PEDIATRICS, 2023, 90 (06): : 626 - 626
  • [37] Case report of severe prenatal presentation of osteogenesis imperfecta caused by uncommon IFITM5 mutation
    Burrill, Natalie
    Coleman, Beverly
    Moldenhauer, Julie
    Khalek, Nahla
    [J]. MOLECULAR GENETICS AND METABOLISM, 2021, 132 : S315 - S315
  • [38] Second-trimester diagnosis of osteogenesis imperfecta associated with schizencephaly by sonography
    Ozkur, Ayhan
    Kervancioglu, Resat
    Kervancioglu, Selim
    Dikensoy, Ebru
    Bayram, Metin
    [J]. SAUDI MEDICAL JOURNAL, 2007, 28 (08) : 1289 - 1290
  • [39] MID-TRIMESTER DIAGNOSIS OF OSTEOGENESIS IMPERFECTA, TYPE-II
    DINNO, ND
    YACOUB, UA
    KADLEC, JF
    GARVER, KL
    [J]. BIRTH DEFECTS-ORIGINAL ARTICLE SERIES, 1982, 18 (3A) : 125 - 132
  • [40] DOMINANT MUTATIONS IN FAMILIAL LETHAL AND SEVERE OSTEOGENESIS IMPERFECTA
    COHENSOLAL, L
    BONAVENTURE, J
    MAROTEAUX, P
    [J]. HUMAN GENETICS, 1991, 87 (03) : 297 - 301