Literature DB >> 20641101

Goldenhar syndrome associated with prenatal maternal Fluoxetine ingestion: Cause or coincidence?

Chantal Farra1, Khalid Yunis, Mohammad Mikati, Nadine Yazbeck, Marianne Majdalani, Johnny Awwad.   

Abstract

Goldenhar syndrome, also known as oculo-auriculo-vertebral spectrum, is a complex, heterogeneous condition characterized by abnormal prenatal development of facial structures. We present the occurrence of Goldenhar syndrome in an infant born to a woman with a history of prenatal Fluoxetine ingestion throughout her pregnancy. Because this is the first reported case associating maternal Fluoxetine intake with fetal craniofacial malformations, a potential mechanism of injury is discussed. The propositus, a male born from nonconsanguinous parents, had facial asymmetry with right microtia and mandibular hypoplasia; he also had bilateral hypoplastic macula, scoliotic deformity of the thoracic spine, and ventricular septal defect. The mother was under treatment with Fluoxetine 20 mg/day prior to conception and maintained the same dosage throughout her pregnancy. The drug is a selective serotonin re-uptake inhibitor, the most widely prescribed for the treatment of depression. The occurrence of developmental aberrations may be caused by a profound serotonin receptor suppressive state in utero leading to aberrant clinical manifestations of the first and second branchial arches. Despite the very many limitations of case reporting of teratogenic events, it remains an important source of information on which more advanced research is based. 2010 Wiley-Liss, Inc.

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Year:  2010        PMID: 20641101     DOI: 10.1002/bdra.20674

Source DB:  PubMed          Journal:  Birth Defects Res A Clin Mol Teratol        ISSN: 1542-0752


  4 in total

1.  Effects of Citalopram on Sutural and Calvarial Cell Processes.

Authors:  Emily Durham; Serena Jen; Lin Wang; Joseph Nasworthy; Mohammed Elsalanty; Seth Weinberg; Jack Yu; James Cray
Journal:  PLoS One       Date:  2015-10-02       Impact factor: 3.240

Review 2.  Genetic Syndromes Associated with Congenital Cardiac Defects and Ophthalmologic Changes - Systematization for Diagnosis in the Clinical Practice.

Authors:  Priscila H A Oliveira; Beatriz S Souza; Eimi N Pacheco; Michele S Menegazzo; Ivan S Corrêa; Paulo R G Zen; Rafael F M Rosa; Claudia C Cesa; Lucia C Pellanda; Manuel A P Vilela
Journal:  Arq Bras Cardiol       Date:  2018-01       Impact factor: 2.000

3.  Prenatal retinoic acid exposure reveals candidate genes for craniofacial disorders.

Authors:  Marie Berenguer; Muriel Darnaudery; Stéphane Claverol; Marc Bonneu; Didier Lacombe; Caroline Rooryck
Journal:  Sci Rep       Date:  2018-11-30       Impact factor: 4.379

4.  A Lebanese family with autosomal recessive oculo-auriculo-vertebral (OAV) spectrum and review of the literature: is OAV a genetically heterogeneous disorder?

Authors:  Chantal Farra; Khaled Yunis; Nadine Yazbeck; Marianne Majdalani; Lama Charafeddine; Rima Wakim; Johnny Awwad
Journal:  Appl Clin Genet       Date:  2011-07-06
  4 in total

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