Literature DB >> 33655927

Two AOS genes attributed to familial exudative vitreoretinopathy with microcephaly: Two case reports.

Zhiyan Tao1, Shaochong Bu2, Fang Lu1.   

Abstract

RATIONALE: Familial exudative vitreoretinopathy (FEVR) is an inherited disorder, which is mostly reported to be associated with the mutation of genes involved in the Wnt signaling pathway related to β-catenin. To the best of our knowledge, the involvement of Adams-Oliver syndrome (AOS) genes in FEVR patients have not been reported before. PATIENT CONCERNS: Two patients with FEVR presented with microcephaly. One of them showed slight scarring of the scalp vertex which is a typical manifestation of AOS. The whole exon sequencing confirmed the diagnosis of AOS with 2 AOS-gene mutations at DOCK6 and ARHGAP31. Further clinical examination revealed that their parents with the same mutations showed FEVR-like vascular anomalies. DIAGNOSIS: Both patients were diagnosed with AOS through whole exon sequencing, and they presented with some FEVR-like retinopathy including retinal detachment.
INTERVENTIONS: Both patients received vitrectomy for tractional retinal detachment with proliferative vitreoretinopathy. During the follow-up, 1 patient received additional laser photocoagulation for tractional retinal detachment. OUTCOMES: The 2 patients remained stable in the latest follow up after the treatment. LESSONS: Microcephaly could be associated with some form of retinopathy. We proposed that mutation of DOCK6 and ARHGAP31 genes could be the possible cause of FEVR associated with microcephaly. Our study suggested that these genes may be candidate genes of FEVR.
Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc.

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Year:  2021        PMID: 33655927      PMCID: PMC7939203          DOI: 10.1097/MD.0000000000024633

Source DB:  PubMed          Journal:  Medicine (Baltimore)        ISSN: 0025-7974            Impact factor:   1.817


  14 in total

1.  Gain-of-function mutations of ARHGAP31, a Cdc42/Rac1 GTPase regulator, cause syndromic cutis aplasia and limb anomalies.

Authors:  Laura Southgate; Rajiv D Machado; Katie M Snape; Martin Primeau; Dimitra Dafou; Deborah M Ruddy; Peter A Branney; Malcolm Fisher; Grace J Lee; Michael A Simpson; Yi He; Teisha Y Bradshaw; Bettina Blaumeiser; William S Winship; Willie Reardon; Eamonn R Maher; David R FitzPatrick; Wim Wuyts; Martin Zenker; Nathalie Lamarche-Vane; Richard C Trembath
Journal:  Am J Hum Genet       Date:  2011-05-13       Impact factor: 11.025

2.  Ocular Manifestations of Cutis Marmorata Telangiectatica Congenita.

Authors:  Vaidehi S Dedania; Omar Moinuddin; Lisa M Lagrou; Sanjana Sathrasala; Flavio Mac Cord Medina; Monte A Del Monte; Emmanuel Y Chang; Brenda L Bohnsack; Cagri G Besirli
Journal:  Ophthalmol Retina       Date:  2019-05-01

3.  Recessive mutations in DOCK6, encoding the guanidine nucleotide exchange factor DOCK6, lead to abnormal actin cytoskeleton organization and Adams-Oliver syndrome.

Authors:  Ranad Shaheen; Eissa Faqeih; Asma Sunker; Heba Morsy; Tarfa Al-Sheddi; Hanan E Shamseldin; Nouran Adly; Mais Hashem; Fowzan S Alkuraya
Journal:  Am J Hum Genet       Date:  2011-08-04       Impact factor: 11.025

4.  Clinical and Molecular Characterization of Familial Exudative Vitreoretinopathy Associated With Microcephaly.

Authors:  Sarah Hull; Gavin Arno; Pia Ostergaard; Nikolas Pontikos; Anthony G Robson; Andrew R Webster; Chris R Hogg; Genevieve A Wright; Robert H H Henderson; Carol-Anne Martin; Andrew P Jackson; Sahar Mansour; Anthony T Moore; Michel Michaelides
Journal:  Am J Ophthalmol       Date:  2019-05-08       Impact factor: 5.258

5.  Mutations in TSPAN12 cause autosomal-dominant familial exudative vitreoretinopathy.

Authors:  James A Poulter; Manir Ali; David F Gilmour; Aine Rice; Hiroyuki Kondo; Kenshi Hayashi; David A Mackey; Lisa S Kearns; Jonathan B Ruddle; Jamie E Craig; Eric A Pierce; Louise M Downey; Moin D Mohamed; Alexander F Markham; Chris F Inglehearn; Carmel Toomes
Journal:  Am J Hum Genet       Date:  2010-02-12       Impact factor: 11.025

6.  Next-generation sequencing and novel variant determination in a cohort of 92 familial exudative vitreoretinopathy patients.

Authors:  Jason Salvo; Vera Lyubasyuk; Mingchu Xu; Hui Wang; Feng Wang; Duy Nguyen; Keqing Wang; Hongrong Luo; Cindy Wen; Catherine Shi; Danni Lin; Kang Zhang; Rui Chen
Journal:  Invest Ophthalmol Vis Sci       Date:  2015-02-24       Impact factor: 4.799

7.  Aplasia cutis congenita associated with limb, eye, and brain anomalies in sibs: a variant of the Adams-Oliver syndrome?

Authors:  K H Orstavik; P Strömme; S Spetalen; T Flage; J Westvik; P Vesterhus; O Skjeldal
Journal:  Am J Med Genet       Date:  1995-10-23

8.  Rac1 activation controls nuclear localization of beta-catenin during canonical Wnt signaling.

Authors:  Ximei Wu; Xiaolin Tu; Kyu Sang Joeng; Matthew J Hilton; David A Williams; Fanxin Long
Journal:  Cell       Date:  2008-04-18       Impact factor: 41.582

9.  Adams Oliver syndrome: A mimicker of familial exudative vitreoretinopathy.

Authors:  Alwaleed M Alsulaiman; Hamad M Alsulaiman; Ahmad Almousa; Sulaiman M Alsulaiman
Journal:  Am J Ophthalmol Case Rep       Date:  2020-04-22

10.  Non-canonical WNT-signaling controls differentiation of lymphatics and extension lymphangiogenesis via RAC and JNK signaling.

Authors:  Grit Lutze; Anna Haarmann; Jules A Demanou Toukam; Kerstin Buttler; Jörg Wilting; Jürgen Becker
Journal:  Sci Rep       Date:  2019-03-18       Impact factor: 4.379

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  1 in total

1.  Synergistic effects of rare variants of ARHGAP31 and FBLN1 in vitro in terminal transverse limb defects.

Authors:  Hong Tian; Fan Chu; Yingjie Li; Mengmeng Xu; Wenjiao Li; Chuanzhou Li
Journal:  Front Genet       Date:  2022-09-13       Impact factor: 4.772

  1 in total

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