Literature DB >> 8849019

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

K H Orstavik1, P Strömme, S Spetalen, T Flage, J Westvik, P Vesterhus, O Skjeldal.   

Abstract

Aplasia cutis congenita (ACC) may occur in isolation or with other congenital malformations. Peripheral limb anomalies and ACC are major elements of the Adams-Oliver syndrome, which is usually inherited as an autosomal dominant disorder. We report on a sister and brother with ACC and brain, eyes, and transverse limb anomalies. The phalanges of the hands and feet were either short or absent. The girl also had absence of right patella, was severely mentally retarded and blind with retinal nonattachment. The boy had a falciform fold in the left eye. He died at age one week and autopsy showed partial agenesis of corpus callosum. The findings in the sibs may represent a severe variant of the Adams-Oliver syndrome, or a previously unrecognized syndrome involving vascular disruption.

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Year:  1995        PMID: 8849019     DOI: 10.1002/ajmg.1320590118

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  5 in total

1.  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

2.  Adams Oliver syndrome: Description of a new phenotype with cerebellar abnormalities in a family.

Authors:  Alessandra D'Amico; Daniela Melis; Felice D'Arco; Nilde Di Paolo; Barbara Carotenuto; Gennaro D'Anna; Carmela Russo; Pasquale Boemio; Arturo Brunetti
Journal:  Pol J Radiol       Date:  2013-11-19

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

4.  Elucidating the genetic architecture of Adams-Oliver syndrome in a large European cohort.

Authors:  Josephina A N Meester; Maja Sukalo; Kim C Schröder; Denny Schanze; Gareth Baynam; Guntram Borck; Nuria C Bramswig; Duygu Duman; Brigitte Gilbert-Dussardier; Muriel Holder-Espinasse; Peter Itin; Diana S Johnson; Shelagh Joss; Hannele Koillinen; Fiona McKenzie; Jenny Morton; Heike Nelle; Willie Reardon; Claudia Roll; Mustafa A Salih; Ravi Savarirayan; Ingrid Scurr; Miranda Splitt; Elizabeth Thompson; Hannah Titheradge; Colm P Travers; Lionel Van Maldergem; Margo Whiteford; Dagmar Wieczorek; Geert Vandeweyer; Richard Trembath; Lut Van Laer; Bart L Loeys; Martin Zenker; Laura Southgate; Wim Wuyts
Journal:  Hum Mutat       Date:  2018-07-04       Impact factor: 4.878

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

Authors:  Zhiyan Tao; Shaochong Bu; Fang Lu
Journal:  Medicine (Baltimore)       Date:  2021-03-05       Impact factor: 1.817

  5 in total

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