Literature DB >> 8867660

Fine-Lubinsky syndrome: a fourth patient with brachycephaly, deafness, cataract, microstomia and mental retardation.

S Aymé1, N Philip.   

Abstract

In 1993, Suthers et al. reported on a child with an undiagnosed syndrome associating developmental delay, brachycephaly, deafness and cataracts. They discussed the possibility that this child had the same dysmorphic syndrome as the patient reported by Fine and Lubinsky in 1983. Twenty years ago, we examined a very similar patient who has been followed up to now. When she was a baby, she looked extremely similar to another patient, reported by Preus et al. in 1984. We now think that these four patients have in fact the same syndrome, the patient reported by Fine and Lubinsky being an example of a very severe expression of this condition, the other patients expressing different anomalies depending on the age at examination.

Entities:  

Mesh:

Year:  1996        PMID: 8867660     DOI: 10.1097/00019605-199601000-00008

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN: 0962-8827            Impact factor:   0.816


  4 in total

Review 1.  Mutation update of transcription factor genes FOXE3, HSF4, MAF, and PITX3 causing cataracts and other developmental ocular defects.

Authors:  Deepti Anand; Smriti A Agrawal; Anne Slavotinek; Salil A Lachke
Journal:  Hum Mutat       Date:  2018-01-16       Impact factor: 4.878

2.  Mutations Impairing GSK3-Mediated MAF Phosphorylation Cause Cataract, Deafness, Intellectual Disability, Seizures, and a Down Syndrome-like Facies.

Authors:  Marcello Niceta; Emilia Stellacci; Karen W Gripp; Giuseppe Zampino; Maria Kousi; Massimiliano Anselmi; Alice Traversa; Andrea Ciolfi; Deborah Stabley; Alessandro Bruselles; Viviana Caputo; Serena Cecchetti; Sabrina Prudente; Maria T Fiorenza; Carla Boitani; Nicole Philip; Dmitriy Niyazov; Chiara Leoni; Takaya Nakane; Kim Keppler-Noreuil; Stephen R Braddock; Gabriele Gillessen-Kaesbach; Antonio Palleschi; Philippe M Campeau; Brendan H L Lee; Celio Pouponnot; Lorenzo Stella; Gianfranco Bocchinfuso; Nicholas Katsanis; Katia Sol-Church; Marco Tartaglia
Journal:  Am J Hum Genet       Date:  2015-04-09       Impact factor: 11.025

3.  Novel missense mutation in the bZIP transcription factor, MAF, associated with congenital cataract, developmental delay, seizures and hearing loss (Aymé-Gripp syndrome).

Authors:  Shari Javadiyan; Jamie E Craig; Shiwani Sharma; Karen M Lower; Theresa Casey; Eric Haan; Emmanuelle Souzeau; Kathryn P Burdon
Journal:  BMC Med Genet       Date:  2017-05-08       Impact factor: 2.103

4.  In Silico Analysis of Possible Interaction between Host Genomic Transcription Factors (TFs) and Zika Virus (ZikaSPH2015) Strain with Combinatorial Gene Regulation; Virus Versus Host-The Game Reloaded.

Authors:  Massimiliano Chetta; Marina Tarsitano; Laura Vicari; Annalisa Saracino; Nenad Bukvic
Journal:  Pathogens       Date:  2021-01-14
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.