Literature DB >> 24568996

Multisegment coloboma in a case of Marfan syndrome: another possible effect of increased TGFβ signaling.

Shannon K LeBlanc1, Deepa Taranath2, Scott Morris3, Christopher P Barnett4.   

Abstract

Colobomata are etiologically heterogeneous and may occur as an isolated defect or as a feature of a variety of single-gene disorders, chromosomal syndromes, or malformation syndromes. Although not classically associated with Marfan syndrome, colobomata have been described in several reports of Marfan syndrome, typically involving the lens and rarely involving other ocular structures. While colobomata of the lens have been described in Marfan syndrome, there are very few reports of coloboma involving other ocular structures. We report a newborn boy presenting with coloboma of the iris, lens, retina, and optic disk who was subsequently diagnosed with Marfan syndrome. Marfan syndrome is a disorder of increased TGFβ signaling, and recent work in the mouse model suggests a role for TGFβ signaling in eye development and coloboma formation, suggesting a causal association between Marfan syndrome and coloboma. Crown
Copyright © 2014. Published by Mosby, Inc. All rights reserved.

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Year:  2014        PMID: 24568996     DOI: 10.1016/j.jaapos.2013.10.017

Source DB:  PubMed          Journal:  J AAPOS        ISSN: 1091-8531            Impact factor:   1.220


  3 in total

1.  Severe aortic root dilatation in infantile Marfan syndrome.

Authors:  Renita A Thomas; Chikamuche T Anyanwu; Maria Blazo; Saradha Subramanian
Journal:  Proc (Bayl Univ Med Cent)       Date:  2019-08-12

2.  Lens coloboma treated with lens surgery.

Authors:  Jia-Kang Wang; Sheng-Hsiang Ma
Journal:  BMJ Case Rep       Date:  2015-09-29

3.  Lens Biometry in Congenital Lens Deformities: A Swept-Source Anterior Segment OCT Analysis.

Authors:  Ze-Xu Chen; Wan-Nan Jia; Yong-Xiang Jiang
Journal:  Front Med (Lausanne)       Date:  2021-12-20
  3 in total

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