Prenatal diagnosis of ring chromosome 6 in a fetus with cerebellar hypoplasia and partial agenesis of corpus callosum: case report and review of the literature

被引:7
|
作者
Andrieux, J [1 ]
Devisme, L
Valat, AS
Robert, Y
Frnka, C
Savary, JB
机构
[1] CHRU, Hop Jean Flandre, Med Genet Lab, F-59037 Lille, France
[2] CHRU Lille, Hop Calmette, Lab Anat & Cytol Pathol, F-59000 Lille, France
[3] CHRU Lille, Hop Jeanne Flandre, Serv Gynecol Obstet, F-59037 Lille, France
[4] CHRU Lille, Hop Jeanne Flandre, Serv Imagerie Med, F-59037 Lille, France
关键词
ring chromosome 6; prenatal diagnosis; corpus callosum agenesis; cerebellar hypoplasia;
D O I
10.1016/j.ejmg.2005.01.028
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Ring chromosome 6 (RC6) is a rare constitutional abnormality, with variable material loss, leading to a variable clinical phenotype: minimal physical anomalies and mild psychomotor retardation to severe physical and mental defects. Among the 22 published cases, only five have been prenatally detected. We describe here a RC6 prenatally diagnosed. Ultrasound follow-up showed growth retardation and cerebellar hypoplasia. Magnetic resonance imaging (MRI) confirmed this, but showed a partial corpus callosum agenesis, leading to amniocentesis and revealing the chromosomal abnormality. Imaging features were correlated with autopsy findings. (c) 2005 Elsevier SAS. All rights reserved.
引用
收藏
页码:199 / 206
页数:8
相关论文
共 50 条
  • [31] Partial hydatidiform mole and coexistent live fetus: a case report and review of the literature
    Zeng, Chengying
    Chen, Yanbi
    Zhao, Lijuan
    Wan, Bo
    OPEN MEDICINE, 2019, 14 (01): : 843 - 846
  • [32] Prenatal diagnosis of distal 13q deletion syndrome in a fetus with esophageal atresia: a case report and review of the literature
    Tomomi Kotani
    Hiroyuki Tsuda
    Yumiko Ito
    Noriyuki Nakamura
    Takafumi Ushida
    Kenji Imai
    Yukako Iitani
    Kazuya Fuma
    Yukako Muramatsu
    Masahiro Hayakawa
    Hiroaki Kajiyama
    Journal of Medical Case Reports, 16
  • [33] Prenatal diagnosis of distal 13q deletion syndrome in a fetus with esophageal atresia: a case report and review of the literature
    Kotani, Tomomi
    Tsuda, Hiroyuki
    Ito, Yumiko
    Nakamura, Noriyuki
    Ushida, Takafumi
    Imai, Kenji
    Iitani, Yukako
    Fuma, Kazuya
    Muramatsu, Yukako
    Hayakawa, Masahiro
    Kajiyama, Hiroaki
    JOURNAL OF MEDICAL CASE REPORTS, 2022, 16 (01)
  • [34] Prenatal diagnosis of FRA10A: A case report and literature review
    De Leon-Luis, J
    Santolaya-Forgas, J
    May, G
    Tonk, V
    Shelton, D
    Galan, I
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2005, 136A (01) : 63 - 65
  • [35] Prenatal diagnosis of pyriform sinus fistula: case report and literature review
    Kakogawa, Jun
    Nako, Takafumi
    Igarashi, Suguru
    Nakamura, Shin
    Tanaka, Mamoru
    CLINICAL CASE REPORTS, 2015, 3 (02): : 106 - 109
  • [36] Prenatal Diagnosis of Coronary Artery Fistula: A Case Report and Review of Literature
    Nagiub, Mohamed
    Mahadin, Deemah
    Gowda, Srinath
    Aggarwal, Sanjeev
    AJP REPORTS, 2014, 4 (02): : E83 - E86
  • [37] Prenatal diagnosis of mediastinal neurenteric cyst: a case report and review of the literature
    Ali Çay
    İbrahim Aydoğdu
    Semih Lütfü Mirapoglu
    Hüseyin Toprak
    Journal of Medical Ultrasonics, 2018, 45 : 633 - 639
  • [38] Prenatal diagnosis of mediastinal neurenteric cyst: a case report and review of the literature
    Cay, Ali
    Aydogdu, Ibrahim
    Mirapoglu, Semih Lutfu
    Toprak, Huseyin
    JOURNAL OF MEDICAL ULTRASONICS, 2018, 45 (04) : 633 - 639
  • [39] Prenatal diagnosis of diastematomyelia and tethered cord - A case report and review of the literature
    Struben, H.
    Visca, E.
    Holzgreve, W.
    Kang, A.
    Hetzel, P.
    Schneider, J.
    Tercanli, S.
    ULTRASCHALL IN DER MEDIZIN, 2008, 29 (01): : 72 - 76
  • [40] Prenatal Diagnosis of Renal Vein Thrombosis: A Case Report and Literature Review
    Moaddab, Amirhossein
    Shamshirsaz, Alireza A.
    Ruano, Rodrigo
    Salmanian, Bahram
    Lee, Wesley
    Belfort, Michael A.
    Espinoza, Jimmy
    FETAL DIAGNOSIS AND THERAPY, 2016, 39 (03) : 228 - 233