Literature DB >> 519897

Retinal manifestations in familial juvenile nephronophthisis.

V Godel, A Iaina, P Nemet, M Lazar.   

Abstract

Three families affected by juvenile nephronophthisis are described and genetically analyzed. The extrarenal manifestations of the disease include retinal findings such as congenital Leber amaurosis, retinitis pigmentosa and sector retinitis pigmentosa. Autosomal recessive transmission and the wide phenotypic spectrum are discussed. The variability in the retinal findings is explained by the presence of a pleiotropic gene with variable expressivity.

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Year:  1979        PMID: 519897     DOI: 10.1111/j.1399-0004.1979.tb01000.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  4 in total

1.  Senior- loken syndrome - a ciliopathy.

Authors:  Hemachandar R
Journal:  J Clin Diagn Res       Date:  2014-11-20

2.  Increased risk of autoimmune hypothyroidism in patients affected by retinitis pigmentosa.

Authors:  G Scanelli; L Dattola; F Padovani
Journal:  J Endocrinol Invest       Date:  1996-03       Impact factor: 4.256

3.  Hereditary renal-retinal dysplasia.

Authors:  V Godel; A Iaina; P Nemet; M Lazar
Journal:  Doc Ophthalmol       Date:  1980-10-15       Impact factor: 2.379

4.  Compound heterozygous splice site variants in the SCLT1 gene highlight an additional candidate locus for Senior-Løken syndrome.

Authors:  Satoshi Katagiri; Takaaki Hayashi; Kazutoshi Yoshitake; Noriyuki Murai; Zenichi Matsui; Hiroyuki Kubo; Hiroyuki Satoh; Senya Matsufuji; Tsuyoshi Takamura; Takashi Yokoo; Yoshihiro Omori; Takahisa Furukawa; Takeshi Iwata; Tadashi Nakano
Journal:  Sci Rep       Date:  2018-11-13       Impact factor: 4.379

  4 in total

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