Literature DB >> 6166737

Coloboma, congenital heart disease, and choanal atresia with multiple anomalies: CHARGE association.

R A Pagon, J M Graham, J Zonana, S L Yong.   

Abstract

We report 21 patients with choanal atresia or ocular coloboma or both who have certain other associated anomalies, including congenital heart disease, postnatal growth deficiency, mental retardation and/or CNS anomalies, microphallus and cryptorchidism, and ear anomalies and/or deafness. Facial palsy, micrognathia, cleft palate, and swallowing difficulties were also common. It has not been possible to define a single etiology or a syndrome in these patients. We propose the mnemonic CHARGE (C-coloboma, H-heart disease, A-atresia choanae, R-retarded growth and retarded development and/or CNS anomalies, G-genital hypoplasia, and E-ear anomalies and/or deafness) to describe the features of this association.

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Mesh:

Year:  1981        PMID: 6166737     DOI: 10.1016/s0022-3476(81)80454-4

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  150 in total

1.  Unilateral semicircular canal aplasia in Goldenhar's syndrome.

Authors:  M M Lemmerling; B D Vanzieleghem; G R Mortier; I J Dhooge; M F Kunnen
Journal:  AJNR Am J Neuroradiol       Date:  2000-08       Impact factor: 3.825

2.  High-resolution in utero 3D MR imaging of inner ear microstructures in fetal sheep.

Authors:  J-H Buhk; M Frisch; J Yamamura; J Graessner; G Adam; U Wedegärtner
Journal:  AJNR Am J Neuroradiol       Date:  2011-10-27       Impact factor: 3.825

3.  The CHARGE association and athyreosis.

Authors:  J F Marín; B García; A Quintana; R Barrio; M T Sordo; C Lozano
Journal:  J Med Genet       Date:  1991-03       Impact factor: 6.318

4.  White sponge naevus and ocular coloboma.

Authors:  S Wright; I S Levy
Journal:  Arch Dis Child       Date:  1991-04       Impact factor: 3.791

5.  Atypical phenotypes associated with pathogenic CHD7 variants and a proposal for broadening CHARGE syndrome clinical diagnostic criteria.

Authors:  Caitlin L Hale; Adrienne N Niederriter; Glenn E Green; Donna M Martin
Journal:  Am J Med Genet A       Date:  2015-11-21       Impact factor: 2.802

6.  Confirmation of CHD7 as a cause of CHARGE association identified by mapping a balanced chromosome translocation in affected monozygotic twins.

Authors:  D Johnson; N Morrison; L Grant; T Turner; J Fantes; J M Connor; V Murday
Journal:  J Med Genet       Date:  2005-08-23       Impact factor: 6.318

7.  CHD7 and retinoic acid signaling cooperate to regulate neural stem cell and inner ear development in mouse models of CHARGE syndrome.

Authors:  Joseph A Micucci; Wanda S Layman; Elizabeth A Hurd; Ethan D Sperry; Sophia F Frank; Mark A Durham; Donald L Swiderski; Jennifer M Skidmore; Peter C Scacheri; Yehoash Raphael; Donna M Martin
Journal:  Hum Mol Genet       Date:  2013-09-10       Impact factor: 6.150

8.  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

9.  Congenital diaphragmatic hernia in CHARGE syndrome.

Authors:  G Casaccia; M C Digilio; P L Seymandi; P Bagolan
Journal:  Pediatr Surg Int       Date:  2007-06-19       Impact factor: 1.827

10.  Oesophageal atresia and associated anomalies.

Authors:  S Chittmittrapap; L Spitz; E M Kiely; R J Brereton
Journal:  Arch Dis Child       Date:  1989-03       Impact factor: 3.791

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