Literature DB >> 950240

Heterogeneity of congenital retinal non-attachment, falciform folds and retinal dysplasia. A guide to genetic counselling.

M Warburg.   

Abstract

The heritable falciform folds and congenital retinal non-attachment reported in the literature are here divided into monosymptomatic and complex types. Of the former, autosomal dominant and recessive disorders are known. The complex types comprise several syndromes, both autosomal recessive and X-linked. Retinal dysplasia is sometimes seen in histological sections from these affections, but it is an unspecific histological reaction, and not a disease sui generis. Attention is drawn to the syndrome with microcephaly, microphthalmia and falciform detachment which, though previously described, has not so far been delineated. It is hypothesized that hydrocephaly and congenital retinal non-attachment with or without microphthalmia and persistent hyperplastic primary vitreous constitute yet another 'new' syndrome, mainly seen in females.

Entities:  

Mesh:

Year:  1976        PMID: 950240     DOI: 10.1159/000152795

Source DB:  PubMed          Journal:  Hum Hered        ISSN: 0001-5652            Impact factor:   0.444


  11 in total

1.  Dominant exudative vitreoretinopathy and other vascular developmental disorders of the peripheral retina.

Authors:  C E van Nouhuys
Journal:  Doc Ophthalmol       Date:  1982-09-23       Impact factor: 2.379

2.  Founder Fukutin mutation causes Walker-Warburg syndrome in four Ashkenazi Jewish families.

Authors:  Wendy Chang; Thomas L Winder; Charles A LeDuc; Lynn L Simpson; William S Millar; Jeffrey Dungan; Norman Ginsberg; Stacey Plaga; Steven A Moore; Wendy K Chung
Journal:  Prenat Diagn       Date:  2009-06       Impact factor: 3.050

3.  Primary vitreoretinal dysplasia transmitted as an autosomal recessive disorder.

Authors:  N Ohba; S Watanabe; S Fujita
Journal:  Br J Ophthalmol       Date:  1981-09       Impact factor: 4.638

4.  Retinal dysplasia.

Authors:  V Godel; P Nemet; M Lazar
Journal:  Doc Ophthalmol       Date:  1981-07-15       Impact factor: 2.379

5.  Probably Norrie's disease due to mutation. Two sporadic sibships of two males each, a necropsy of one case, and, given Norrie's disease, a calculation of the gene mutation frequency.

Authors:  C I Phillips; M Newton; J Duvall; S Holloway; A M Levy
Journal:  Br J Ophthalmol       Date:  1986-04       Impact factor: 4.638

6.  Increased apoptosis of myoblasts in Drosophila model for the Walker-Warburg syndrome.

Authors:  Morio Ueyama; Yoshihiro Akimoto; Tomomi Ichimiya; Ryu Ueda; Hayato Kawakami; Toshiro Aigaki; Shoko Nishihara
Journal:  PLoS One       Date:  2010-07-13       Impact factor: 3.240

Review 7.  Walker-Warburg syndrome.

Authors:  Jiri Vajsar; Harry Schachter
Journal:  Orphanet J Rare Dis       Date:  2006-08-03       Impact factor: 4.123

8.  The Genetic Causes of Nonsyndromic Congenital Retinal Detachment: A Genetic and Phenotypic Study of Pakistani Families.

Authors:  Vafa Keser; Ayesha Khan; Sorath Siddiqui; Irma Lopez; Huanan Ren; Raheel Qamar; Javad Nadaf; Jacek Majewski; Rui Chen; Robert K Koenekoop
Journal:  Invest Ophthalmol Vis Sci       Date:  2017-02-01       Impact factor: 4.799

Review 9.  The role of defective glycosylation in congenital muscular dystrophy.

Authors:  Harry Schachter; Jiri Vajsar; Wenli Zhang
Journal:  Glycoconj J       Date:  2004       Impact factor: 3.009

10.  Retinal and optic nerve changes in microcephaly: An optical coherence tomography study.

Authors:  Eleni Papageorgiou; Anastasia Pilat; Frank Proudlock; Helena Lee; Ravi Purohit; Viral Sheth; Pradeep Vasudevan; Irene Gottlob
Journal:  Neurology       Date:  2018-07-11       Impact factor: 9.910

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.