Literature DB >> 10590394

CHARGE Association in newborns: a registry-based study.

K Källén1, E Robert, P Mastroiacovo, E E Castilla, B Källén.   

Abstract

The CHARGE Association is a nonrandom occurrence of congenital malformations that has been described in clinical series. Reported patients have been selected on the basis of certain prior criteria. In this article, we try to identify a congenital malformation pattern corresponding to the CHARGE Association, using statistical methods and analyzing 5,260 infants with multiple malformations collected from four large registries of congenital malformations. Care was taken to identify a number of confounding characteristics that can influence the ascertainment and registration of specific congenital malformations. We have identified a cluster of malformations that generally agreed with the current clinical definition of the CHARGE Association and have added some further malformations (e.g., facial clefts). We demonstrate that others (e.g. , esophageal atresia) are probably not part of the pattern. Heart defects (H in the acronym) seems to be less helpful in identifying infants with the association. We suggest a method to select infants who probably represent the CHARGE Association for analyses of possible risk factors. Copyright 1999 Wiley-Liss, Inc.

Entities:  

Mesh:

Year:  1999        PMID: 10590394     DOI: 10.1002/(SICI)1096-9926(199912)60:6<334::AID-TERA5>3.0.CO;2-S

Source DB:  PubMed          Journal:  Teratology        ISSN: 0040-3709


  16 in total

Review 1.  Chromodomain proteins in development: lessons from CHARGE syndrome.

Authors:  W S Layman; E A Hurd; D M Martin
Journal:  Clin Genet       Date:  2010-04-08       Impact factor: 4.438

2.  Genomic distribution of CHD7 on chromatin tracks H3K4 methylation patterns.

Authors:  Michael P Schnetz; Cynthia F Bartels; Kuntal Shastri; Dheepa Balasubramanian; Gabriel E Zentner; Ravishankar Balaji; Xiaodong Zhang; Lingyun Song; Zhenghe Wang; Thomas Laframboise; Gregory E Crawford; Peter C Scacheri
Journal:  Genome Res       Date:  2009-02-27       Impact factor: 9.043

3.  Epigenetic Developmental Disorders: CHARGE syndrome, a case study.

Authors:  Donna M Martin
Journal:  Curr Genet Med Rep       Date:  2015-03

4.  Mutations in the CHD7 gene: the experience of a commercial laboratory.

Authors:  Cynthia F Bartels; Cheryl Scacheri; Lashonda White; Peter C Scacheri; Sherri Bale
Journal:  Genet Test Mol Biomarkers       Date:  2010-12

5.  Modeling human craniofacial disorders in Xenopus.

Authors:  Aditi Dubey; Jean-Pierre Saint-Jeannet
Journal:  Curr Pathobiol Rep       Date:  2017-01-24

6.  Autism with ophthalmologic malformations: the plot thickens.

Authors:  Marilyn T Miller; Kerstin Strömland; Liana Ventura; Maria Johansson; Jose M Bandim; Christopher Gillberg
Journal:  Trans Am Ophthalmol Soc       Date:  2004

7.  Defects in neural stem cell proliferation and olfaction in Chd7 deficient mice indicate a mechanism for hyposmia in human CHARGE syndrome.

Authors:  W S Layman; D P McEwen; L A Beyer; S R Lalani; S D Fernbach; E Oh; A Swaroop; C C Hegg; Y Raphael; J R Martens; D M Martin
Journal:  Hum Mol Genet       Date:  2009-03-11       Impact factor: 6.150

8.  Olfactory anomalies in CHARGE syndrome: imaging findings of a potential major diagnostic criterion.

Authors:  J Blustajn; C F E Kirsch; A Panigrahy; I Netchine
Journal:  AJNR Am J Neuroradiol       Date:  2008-04-16       Impact factor: 3.825

9.  Preferential associated anomalies in 818 cases of microtia in South America.

Authors:  Daniela V Luquetti; Timothy C Cox; Jorge Lopez-Camelo; Maria da Graça Dutra; Michael L Cunningham; Eduardo E Castilla
Journal:  Am J Med Genet A       Date:  2013-03-29       Impact factor: 2.802

Review 10.  Nervous system development and disease: A focus on trithorax related proteins and chromatin remodelers.

Authors:  Amanda Moccia; Donna M Martin
Journal:  Mol Cell Neurosci       Date:  2017-11-28       Impact factor: 4.314

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