Literature DB >> 15633180

CHARGE association in Sweden: malformations and functional deficits.

Kerstin Strömland1, Lotta Sjögreen, Maria Johansson, Britt-Marie Ekman Joelsson, Marilyn Miller, Susanna Danielsson, Eva Billstedt, Christopher Gillberg, Catharina Jacobsson, Jan Andersson Norinder, Gösta Granström.   

Abstract

CHARGE association (CA) consists of a non-random association of ocular coloboma (C), heart anomaly (H), atresia of choanae (A), retarded growth and/or development (R), genital hypoplasia (G), and ear anomalies and/or hearing impairment (E). A prospective multidisciplinary study of 31 Swedish patients with CA was undertaken in order to describe the associated malformations and functional deficits, find possible etiological factors and identify critical time periods for the maldevelopment. The clinical files were analyzed, the mothers answered a questionnaire on history of prenatal events, and a clinical evaluation of systemic findings, vision, hearing, balance, speech, oral and swallowing function, and neuro-psychiatric function, especially autism, was performed. The most frequent physical abnormalities affected ears (90%), eyes (90%), brain (61%), heart (52%), retarded growth (48%), genitals (38%), choanae (35%), and facial nerve (32%). Sixty-one percent of the patients were visually impaired or blind, and 74% had hearing loss or deafness. Problems in balance, speech, and eating were common. Forty percent of the patients had autism/atypical autism, and 82% had developmental delay. Three children were born following assisted fertilization and two mothers had diabetes. The mothers reported infections, bleedings, and drug use during pregnancy. Analysis of possible critical time periods suggested that most malformations were produced early in pregnancy, mainly during post conceptual weeks 4, 5, and 6. A multidisciplinary approach is essential in the assessment and management of CA. Copyright (c) 2005 Wiley-Liss, Inc.

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Year:  2005        PMID: 15633180     DOI: 10.1002/ajmg.a.30563

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  8 in total

1.  CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene.

Authors:  M C J Jongmans; R J Admiraal; K P van der Donk; L E L M Vissers; A F Baas; L Kapusta; J M van Hagen; D Donnai; T J de Ravel; J A Veltman; A Geurts van Kessel; B B A De Vries; H G Brunner; L H Hoefsloot; C M A van Ravenswaaij
Journal:  J Med Genet       Date:  2005-09-09       Impact factor: 6.318

2.  Visual electrophysiological findings in CHARGE syndrome with bilateral colobomas: a case report.

Authors:  R Hamilton; P Gonzalez; J Dudgeon; H Mactier
Journal:  Doc Ophthalmol       Date:  2010-03-09       Impact factor: 2.379

3.  Care of Children with DiGeorge Before and After Cultured Thymus Tissue Implantation.

Authors:  Stephanie E Gupton; Elizabeth A McCarthy; M Louise Markert
Journal:  J Clin Immunol       Date:  2021-05-18       Impact factor: 8.542

4.  CHARGE syndrome-associated proteins FAM172A and CHD7 influence male sex determination and differentiation through transcriptional and alternative splicing mechanisms.

Authors:  Catherine Bélanger; Tatiana Cardinal; Elizabeth Leduc; Robert S Viger; Nicolas Pilon
Journal:  FASEB J       Date:  2022-03       Impact factor: 5.834

Review 5.  Phenotypic characteristics and variability in CHARGE syndrome: a PRISMA compliant systematic review and meta-analysis.

Authors:  Andrea T Thomas; Jane Waite; Caitlin A Williams; Jeremy Kirk; Chris Oliver; Caroline Richards
Journal:  J Neurodev Disord       Date:  2022-08-31       Impact factor: 4.074

Review 6.  Eyes on CHARGE syndrome: Roles of CHD7 in ocular development.

Authors:  Laura A Krueger; Ann C Morris
Journal:  Front Cell Dev Biol       Date:  2022-09-08

7.  Visual Function and Ophthalmological Findings in CHARGE Syndrome: Revision of Literature, Definition of a New Clinical Spectrum and Genotype Phenotype Correlation.

Authors:  Roberta Onesimo; Daniela Ricci; Cristiana Agazzi; Simona Leone; Maria Petrianni; Lorenzo Orazi; Filippo Amore; Annabella Salerni; Chiara Leoni; Daniela Chieffo; Marco Tartaglia; Eugenio Mercuri; Giuseppe Zampino
Journal:  Genes (Basel)       Date:  2021-06-25       Impact factor: 4.096

Review 8.  Congenital heart defects in CHARGE: The molecular role of CHD7 and effects on cardiac phenotype and clinical outcomes.

Authors:  Joshua K Meisner; Donna M Martin
Journal:  Am J Med Genet C Semin Med Genet       Date:  2019-12-13       Impact factor: 3.359

  8 in total

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