Literature DB >> 15800906

Autosomal dominant microtia and ocular coloboma: new syndrome or an extension of the oculo-auriculo-vertebral spectrum?

Anita E Beck1, Louanne Hudgins, H Eugene Hoyme.   

Abstract

The oculo-auriculo-vertebral (OAV) spectrum is an etiologically heterogeneous condition classically consisting of microtia, hemifacial microsomia, epibulbar dermoids, and vertebral anomalies. Other eye findings described in OAV include upper eyelid colobomas, ptosis, and varying degrees of microphthalmia or even anophthalmia. Iris and/or retinal colobomas have rarely been reported. We describe two familial cases of apparent OAV with ocular colobomas. We postulate that iris and/or retinal colobomas associated with OAV may represent a subgroup within the OAV spectrum with autosomal dominant inheritance, as in the families described herein. Since microtia can result from aberrant migration of neural crest cells into the first and second branchial arches during early embryonic development, and concomitant deficient neural crest migration into the developing eye can lead to ocular coloboma and or iris heterochromia, it may be that the altered gene or genes in our familial cases are involved with regulation of neural crest development. 2005 Wiley-Liss, Inc.

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Year:  2005        PMID: 15800906     DOI: 10.1002/ajmg.a.30638

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


  6 in total

1.  Distinctive spine abnormalities in patients with Goldenhar syndrome: tomographic assessment.

Authors:  Ali Al Kaissi; Farid Ben Chehida; Rudolf Ganger; Klaus Klaushofer; Franz Grill
Journal:  Eur Spine J       Date:  2014-02-07       Impact factor: 3.134

2.  A locus for autosomal dominant accessory auricular anomaly maps to 14q11.2-q12.

Authors:  Yongjia Yang; Jihong Guo; Zheng Liu; Siyuan Tang; Ningdong Li; Mengrong Yang; Qiong Pang; Feiyue Fan; Juan Bu; Song Tao Yuan; Xiangjun Xiao; Yuxiang Chen; Kanxing Zhao
Journal:  Hum Genet       Date:  2006-06-15       Impact factor: 4.132

Review 3.  The eye as an organizer of craniofacial development.

Authors:  Phillip E Kish; Brenda L Bohnsack; Donika Gallina; Daniel S Kasprick; Alon Kahana
Journal:  Genesis       Date:  2011-04-01       Impact factor: 2.487

4.  Hemifacial microsomia with pulmonary hypoplasia.

Authors:  Inusha Panigrahi; Rashmi Ranjan Das; Ram Kumar Marwaha
Journal:  BMJ Case Rep       Date:  2010-05-16

5.  Identification of sequence variants associated with severe microtia-astresia by targeted sequencing.

Authors:  Pu Wang; Yibei Wang; Xinmiao Fan; Yaping Liu; Yue Fan; Tao Liu; Chongjian Chen; Shuyang Zhang; Xiaowei Chen
Journal:  BMC Med Genomics       Date:  2019-01-28       Impact factor: 3.063

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
  6 in total

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