Association between Beckwith-Wiedemann syndrome and assisted reproductive technology: a case series of 19 patients

被引:144
|
作者
Chang, AS
Moley, KH
Wangler, MDM
Feinberg, AP
DeBaun, MR
机构
[1] Washington Univ, Sch Med, Div Genet, St Louis, MO 63108 USA
[2] Johns Hopkins Univ, Sch Med, Dept Obstet & Gynecol, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA
[4] Johns Hopkins Univ, Sch Med, Dept Oncol, Baltimore, MD 21205 USA
[5] Johns Hopkins Univ, Sch Med, Dept Mol Biol & Genet, Baltimore, MD 21205 USA
关键词
Beckwith-Wiedemann syndrome; assisted reproductive technology; in vitro fertilization;
D O I
10.1016/j.fertnstert.2004.07.964
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: An association between assisted reproductive technique (ART) and specific imprinting mutations, such as Beckwith-Wiedemann syndrome (BWS), has recently been documented. Based on experiments in farm animals that demonstrated an association between alterations in culture media during ART and large offspring syndrome, we hypothesized that the culture media could be implicated as a common factor among the children with BWS conceived after ART. Design: Retrospective case series. Setting: Registry from Academic Medical Center. Patient(s): Nineteen children born after ART were identified within the registry. Main Outcome Measure(S): Demographics of patients, type of ART, culture media, IVF parameters. Result(S): Twelve of the 19 medical records from the reproductive endocrine centers were successfully obtained. Ten of 12 mothers of children with BWS had lVF, but no single, consistent culture media was used in this group. Half of the patients underwent IVF with intracytoplasmic sperm injection (ICSI; n = 5), whereas the other half had routine IVF. One child was conceived through clorniphene citrate (CC) stimulation and artificial insemination, whereas another patient conceived through gonadotropin stimulation with intrauterine insemination (IUI). The gonadotropin dosage and quantity of embryos transferred also varied significantly. The only consistent finding was that all 12 women received some type of ovarian stimulation medication. Conclusion(s): Large epidenniologic studies are needed to further study the association between BWS and ART. (Fertil Steril((R)) 2005;83:349-54. (C) 2005 by American Society for Reproductive Medicine.)
引用
收藏
页码:349 / 354
页数:6
相关论文
共 50 条
  • [41] Pancreatoblastoma associated with incomplete Beckwith-Wiedemann syndrome:: case report and review of the literature
    Muguerza, R
    Rodriguez, A
    Formigo, E
    Montero, M
    Vázquez, JL
    Páramo, C
    Campos, C
    JOURNAL OF PEDIATRIC SURGERY, 2005, 40 (08) : 1341 - 1344
  • [42] Investigation of a pervasive immune, cardiac, and behavioral phenotype in Beckwith-Wiedemann syndrome: A case report
    McElroy, Timothy D.
    Duffy, Kelly A.
    Hathaway, Evan R.
    Byrne, Mallory E.
    Kalish, Jennifer M.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2023, 191 (04) : 1107 - 1110
  • [43] Beckwith-Wiedemann syndrome associated with a renal abscess. Report of a case and review of the literature
    Martin Palacios-Acosta, Jose
    Echavez-del Riego, Jaen
    Shalkow-Klincovstein, Jaime
    Alejandro Leal-Leal, Carlos
    Oldak-Skvirsky, David
    Leon-Hernandez, Angelica
    ACTA PEDIATRICA DE MEXICO, 2012, 33 (04): : 170 - 174
  • [44] Fibroepithelial Breast Tumors in a Teenager with Beckwith-Wiedemann Syndrome: A Case Report and Review of Literature
    Oktay, Aysenur
    Esmat, Habib Ahmad
    Aslan, Ozge
    EUROPEAN JOURNAL OF BREAST HEALTH, 2021, 17 (03) : 288 - 291
  • [45] Novel mutations of CDKN1C in Japanese patients with Beckwith-Wiedemann syndrome
    Yatsuki, Hitomi
    Higashimoto, Ken
    Jozaki, Kosuke
    Koide, Kayoko
    Okada, Junichiro
    Watanabe, Yoriko
    Okamoto, Nobuhiko
    Tsuno, Yoshinobu
    Yoshida, Yoko
    Ueda, Kazutoshi
    Shimizu, Kenji
    Ohashi, Hirofumi
    Mukai, Tsunehiro
    Soejima, Hidenobu
    GENES & GENOMICS, 2013, 35 (02) : 141 - 147
  • [46] Detection of hypermethylation at H19DMR at amniocentesis in a fetus with overgrowth, distended abdomen and Beckwith-Wiedemann syndrome
    Chen, Chih-Ping
    Chern, Schu-Rern
    Lin, Chien-Hsing
    Hsu, Chin-Yuan
    Lin, Hsiang-Yu
    Wu, Fang-Tzu
    Chen, Shin-Wen
    Wang, Wayseen
    TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2021, 60 (06): : 1103 - 1106
  • [47] Novel mutations of CDKN1C in Japanese patients with Beckwith-Wiedemann syndrome
    Hitomi Yatsuki
    Ken Higashimoto
    Kosuke Jozaki
    Kayoko Koide
    Junichiro Okada
    Yoriko Watanabe
    Nobuhiko Okamoto
    Yoshinobu Tsuno
    Yoko Yoshida
    Kazutoshi Ueda
    Kenji Shimizu
    Hirofumi Ohashi
    Tsunehiro Mukai
    Hidenobu Soejima
    Genes & Genomics, 2013, 35 : 141 - 147
  • [48] Quantitative DNA Methylation Analysis and Epigenotype-Phenotype Correlations in Taiwanese Patients with Beckwith-Wiedemann Syndrome
    Lin, Hsiang-Yu
    Lee, Chung-Lin
    Fran, Sisca
    Tu, Ru-Yi
    Chang, Ya-Hui
    Niu, Dau-Ming
    Chang, Chia-Ying
    Chiu, Pao Chin
    Chou, Yen-Yin
    Hsiao, Hui-Pin
    Yang, Chia-Feng
    Tsai, Meng-Che
    Chu, Tzu-Hung
    Chuang, Chih-Kuang
    Lin, Shuan-Pei
    JOURNAL OF PERSONALIZED MEDICINE, 2021, 11 (11):
  • [49] Associations between the timing of tongue reduction surgery, (Epi) genotype, and dentoskeletal development in patients with Beckwith-Wiedemann syndrome
    Wagner, Connor S.
    Pontell, Matthew E.
    Barrero, Carlos E.
    Salinero, Lauren K.
    Low, David W.
    Liao, Eric C.
    Nah, Hyun-Duck
    Kalish, Jennifer M.
    Taylor, Jesse A.
    JOURNAL OF CRANIO-MAXILLOFACIAL SURGERY, 2023, 51 (09) : 568 - 573
  • [50] CDKN1C expression in Beckwith-Wiedemann syndrome patients with allele imbalance
    Algar, EM
    Deeble, GJ
    Smith, PJ
    JOURNAL OF MEDICAL GENETICS, 1999, 36 (07) : 524 - 531