Literature DB >> 20104598

Non-genetic risk factors for holoprosencephaly.

Candice Y Johnson1, Sonja A Rasmussen.   

Abstract

Holoprosencephaly (HPE) is a congenital defect of the brain characterized by incomplete cleavage of the embryonic forebrain into left and right hemispheres. Although a substantial proportion of cases of HPE can be attributed to genetic abnormalities, the etiology in many cases remains unknown, with non-genetic risk factors believed to be important contributors. Due to the low birth prevalence of this defect, it has proven difficult to conduct studies of sufficient size to identify risk factors with certainty. This article provides a summary of non-genetic risk factors for HPE that have been investigated in case reports and case series, animal studies, and epidemiologic studies, including maternal illnesses, therapeutic and non-therapeutic exposures, nutritional factors, and sociodemographic factors. The article also highlights challenges in study design and further areas for research to better understand the etiology of HPE. 2010 Wiley-Liss, Inc.

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Year:  2010        PMID: 20104598     DOI: 10.1002/ajmg.c.30242

Source DB:  PubMed          Journal:  Am J Med Genet C Semin Med Genet        ISSN: 1552-4868            Impact factor:   3.908


  22 in total

Review 1.  Cyclopia: an epidemiologic study in a large dataset from the International Clearinghouse of Birth Defects Surveillance and Research.

Authors:  Iêda M Orioli; Emmanuelle Amar; Marian K Bakker; Eva Bermejo-Sánchez; Fabrizio Bianchi; Mark A Canfield; Maurizio Clementi; Adolfo Correa; Melinda Csáky-Szunyogh; Marcia L Feldkamp; Danielle Landau; Emanuele Leoncini; Zhu Li; R Brian Lowry; Pierpaolo Mastroiacovo; Margery Morgan; Osvaldo M Mutchinick; Anke Rissmann; Annukka Ritvanen; Gioacchino Scarano; Elena Szabova; Eduardo E Castilla
Journal:  Am J Med Genet C Semin Med Genet       Date:  2011-10-17       Impact factor: 3.908

Review 2.  The Learning Disabilities Network (LeaDNet): using neurofibromatosis type 1 (NF1) as a paradigm for translational research.

Authors:  Maria T Acosta; Carrie E Bearden; F Xavier Castellanos; Xavier F Castellanos; Laurie Cutting; Ype Elgersma; Gerard Gioia; David H Gutmann; Yong-Seok Lee; Eric Legius; Maximillian Muenke; Kathryn North; Luis F Parada; Nancy Ratner; Kim Hunter-Schaedle; Alcino J Silva
Journal:  Am J Med Genet A       Date:  2012-07-20       Impact factor: 2.802

3.  New findings for phenotype-genotype correlations in a large European series of holoprosencephaly cases.

Authors:  Sandra Mercier; Christèle Dubourg; Nicolas Garcelon; Boris Campillo-Gimenez; Isabelle Gicquel; Marion Belleguic; Leslie Ratié; Laurent Pasquier; Philippe Loget; Claude Bendavid; Sylvie Jaillard; Lucie Rochard; Chloé Quélin; Valérie Dupé; Véronique David; Sylvie Odent
Journal:  J Med Genet       Date:  2011-09-22       Impact factor: 6.318

Review 4.  Animal models of gene-alcohol interactions.

Authors:  Charles Benjamin Lovely
Journal:  Birth Defects Res       Date:  2019-11-27       Impact factor: 2.344

5.  White Matter Injury and Structural Anomalies in Infants with Prenatal Opioid Exposure.

Authors:  S L Merhar; N A Parikh; A Braimah; B B Poindexter; J Tkach; B Kline-Fath
Journal:  AJNR Am J Neuroradiol       Date:  2019-10-17       Impact factor: 3.825

Review 6.  Holoprosencephaly: a guide to diagnosis and clinical management.

Authors:  Manu S Raam; Benjamin D Solomon; Maximilian Muenke
Journal:  Indian Pediatr       Date:  2011-06       Impact factor: 1.411

Review 7.  Holoprosencephaly: signaling interactions between the brain and the face, the environment and the genes, and the phenotypic variability in animal models and humans.

Authors:  Anna Petryk; Daniel Graf; Ralph Marcucio
Journal:  Wiley Interdiscip Rev Dev Biol       Date:  2014-10-22       Impact factor: 5.814

Review 8.  Holoprosencephaly: recommendations for diagnosis and management.

Authors:  Emily F Kauvar; Maximilian Muenke
Journal:  Curr Opin Pediatr       Date:  2010-12       Impact factor: 2.856

9.  Gene-ethanol interactions underlying fetal alcohol spectrum disorders.

Authors:  Neil McCarthy; Johann K Eberhart
Journal:  Cell Mol Life Sci       Date:  2014-02-20       Impact factor: 9.261

Review 10.  Modeling the complex etiology of holoprosencephaly in mice.

Authors:  Mingi Hong; Robert S Krauss
Journal:  Am J Med Genet C Semin Med Genet       Date:  2018-05-11       Impact factor: 3.908

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