Literature DB >> 8818446

Oculo-auriculo-vertebral spectrum and the CHARGE association: clinical evidence for a common pathogenetic mechanism.

T D Van Meter1, D D Weaver.   

Abstract

We describe two infants with features of both the oculo-auriculo-vertebral spectrum (OAVS) and the CHARGE association (CA). Both patients are more severely affected than the typical patient with the OAVS. Each has facial asymmetry, mandibular hypoplasia, ear abnormalities, hearing impairment, microphthalmia, heart defects, and developmental delay. They also have features that are not characteristic of either OAVS or CA including torticollis, plagiocephaly, and heminostril. Based on the findings of these patients and other reported in the literature, there appears to be a significant overlap of features between OAVS and CA, and we suggest that these conditions in fact may be produced by the same pathogenetic mechanism. One such mechanism to explain the overlap of these disorders is that both conditions are part of the axial mesodermal spectrum, and represent a dysblastogenetic process. This mechanism may also explain the presence of some of the additional features not normally seen in OAVs and CA but seen in these two infants.

Entities:  

Mesh:

Year:  1996        PMID: 8818446

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN: 0962-8827            Impact factor:   0.816


  7 in total

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Authors:  M M Lemmerling; B D Vanzieleghem; G R Mortier; I J Dhooge; M F Kunnen
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2.  More Clinical Overlap between 22q11.2 Deletion Syndrome and CHARGE Syndrome than Often Anticipated.

Authors:  N Corsten-Janssen; S C Saitta; L H Hoefsloot; D M McDonald-McGinn; D A Driscoll; R Derks; K A Dickinson; W S Kerstjens-Frederikse; B S Emanuel; E H Zackai; C M A van Ravenswaaij-Arts
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3.  Autism with ophthalmologic malformations: the plot thickens.

Authors:  Marilyn T Miller; Kerstin Strömland; Liana Ventura; Maria Johansson; Jose M Bandim; Christopher Gillberg
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4.  CHD7, the gene mutated in CHARGE syndrome, regulates genes involved in neural crest cell guidance.

Authors:  Yvonne Schulz; Peter Wehner; Lennart Opitz; Gabriela Salinas-Riester; Ernie M H F Bongers; Conny M A van Ravenswaaij-Arts; Josephine Wincent; Jacqueline Schoumans; Jürgen Kohlhase; Annette Borchers; Silke Pauli
Journal:  Hum Genet       Date:  2014-04-13       Impact factor: 4.132

5.  Role of Chd7 in zebrafish: a model for CHARGE syndrome.

Authors:  Shunmoogum A Patten; Nicole L Jacobs-McDaniels; Charlotte Zaouter; Pierre Drapeau; R Craig Albertson; Florina Moldovan
Journal:  PLoS One       Date:  2012-02-20       Impact factor: 3.240

6.  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

7.  Goldenhar Syndrome: A rare case report.

Authors:  Ruchi Bhuyan; Abhishek Ranjan Pati; Sanat Kumar Bhuyan; Bikash Bishwadarshee Nayak
Journal:  J Oral Maxillofac Pathol       Date:  2016 May-Aug
  7 in total

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