Literature DB >> 16586236

Adams-Oliver syndrome associated with cutis marmorata telangiectatica congenita and congenital cataract: a case report.

Laurence Fayol1, Patricia Garcia, Danièle Denis, Nicole Philip, Umberto Simeoni.   

Abstract

A female infant presented with Adams-Oliver syndrome (AOS), intrauterine growth retardation, severe cutis marmorata telangiectatica congenita, bilateral congenital cataract, and periventricular lesions. The here-reported association of bilateral congenital cataract with AOS is original. Adams-Oliver syndrome is a genetic defect that causes a vasculopathy and leads to a variety of phenotypes. This observation further supports the current understanding of the physiopathology of AOS.

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Year:  2006        PMID: 16586236     DOI: 10.1055/s-2006-934099

Source DB:  PubMed          Journal:  Am J Perinatol        ISSN: 0735-1631            Impact factor:   1.862


  3 in total

1.  MRI of the fetal eyes: morphologic and biometric assessment for abnormal development with ultrasonographic and clinicopathologic correlation.

Authors:  Ashley J Robinson; Susan Blaser; Ants Toi; David Chitayat; Sophie Pantazi; Sarah Keating; Sandra Viero; Greg Ryan
Journal:  Pediatr Radiol       Date:  2008-07-17

2.  Atypical Adams-Oliver syndrome with typical ocular signs of familial exudative vitreoretinopathy.

Authors:  En-Zhong Jin; Lyu-Zhen Huang; Ming-Wei Zhao; Hong Yin
Journal:  Int J Ophthalmol       Date:  2022-08-18       Impact factor: 1.645

3.  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
  3 in total

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