Literature DB >> 16532152

Monozygotic twins discordant for Goldenhar syndrome.

Leonardo Lima Verona1, Nicholas Godoy Canazza Damian, Lucimara P Pavarina, Cristina H F Ferreira, Débora Gusmão Melo.   

Abstract

OBJECTIVE: To report on a pair of monozygotic female twins discordant for Goldenhar syndrome. DESCRIPTION: The affected twin was a girl, who was delivered by caesarean section at 35 weeks' gestation. Her birth weight was 2,170 g, length 42.5 cm, head circumference 30 cm and her Apgar scores were 3/7. After birth the child developed severe respiratory distress and had to be moved to the neonatal intensive care unit (ICU). The other twin was a girl, born weighing 3,200 g with a length of 49 cm, head circumference of 34 cm and Apgar scores of 8/10. She was transferred to the mother-baby unit soon after birth and was discharged two days later. There was no consanguinity between the twins' parents, who were young and healthy at the time of their conception. The affected child's dysmorphic features included left hemifacial microsomia, severe micrognathia, abnormal ears, bilateral preauricular tags and epibulbar dermoid in the right eye. She developed obstructive apnea due to micrognathia and required tracheostomy. Abdominal and cranial ultrasound findings were normal, as was an ophthalmological assessment. Spine x-ray showed hemivertebra at T9 and T10. An echocardiogram showed Tetralogy of Fallot. GTG-banded karyotyping was performed on peripheral blood cells and revealed 46,XX. Zygosity testing established the pair of twins to be monozygotic with a probability greater than 99:1. COMMENT: Goldenhar syndrome was diagnosed in one of the twins described here. There are several reports of twins discordant for this disorder and therefore non-genetic factors may also play an important role, for instance vascular disruption during morphogenesis.

Entities:  

Mesh:

Year:  2006        PMID: 16532152     DOI: 10.2223/JPED.1441

Source DB:  PubMed          Journal:  J Pediatr (Rio J)        ISSN: 0021-7557            Impact factor:   2.197


  6 in total

Review 1.  Microarray-Based Comparative Genomic Hybridization, Multiplex Ligation-Dependent Probe Amplification, and High-Resolution Karyotype for Differential Diagnosis Oculoauriculovertebral Spectrum: A Systematic Review.

Authors:  Andressa Barreto Glaeser; Bruna Lixinski Diniz; Desirée Deconte; Andressa Schneiders Santos; Rafael Fabiano Machado Rosa; Paulo Ricardo Gazzola Zen
Journal:  J Pediatr Genet       Date:  2020-05-27

2.  Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells.

Authors:  Jet Bliek; Marielle Alders; Saskia M Maas; Roelof-Jan Oostra; Deborah M Mackay; Karin van der Lip; Johnatan L Callaway; Alice Brooks; Sandra van 't Padje; Andries Westerveld; Nico J Leschot; Marcel M A M Mannens
Journal:  Eur J Hum Genet       Date:  2009-06-10       Impact factor: 4.246

3.  Vasoactive exposures during pregnancy and risk of microtia.

Authors:  Carla M Van Bennekom; Allen A Mitchell; Cynthia A Moore; Martha M Werler
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2012-11-24

4.  Case report: Goldenhar syndrome following donor oocyte IVF.

Authors:  Victoria Gittins; Jason Kasraie
Journal:  J Assist Reprod Genet       Date:  2010-06-23       Impact factor: 3.412

5.  Reproduction abnormalities and twin pregnancies in parents of sporadic patients with oculo-auriculo-vertebral spectrum/Goldenhar syndrome.

Authors:  Dagmar Wieczorek; Michael Ludwig; Stefan Boehringer; Piet Hein Jongbloet; Gabriele Gillessen-Kaesbach; Bernhard Horsthemke
Journal:  Hum Genet       Date:  2007-02-13       Impact factor: 5.881

6.  Whole-Exome Sequencing of Discordant Monozygotic Twin Families for Identification of Candidate Genes for Microtia-Atresia.

Authors:  Xinmiao Fan; Lu Ping; Hao Sun; Yushan Chen; Pu Wang; Tao Liu; Rui Jiang; Xuegong Zhang; Xiaowei Chen
Journal:  Front Genet       Date:  2020-10-22       Impact factor: 4.599

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.