Literature DB >> 6696034

Leber's congenital amaurosis associated with familial juvenile nephronophthisis and cone-shaped epiphyses of the hands (the Saldino-Mainzer syndrome).

D S Ellis, J R Heckenlively, C L Martin, R S Lachman, N A Sakati, D L Rimoin.   

Abstract

Three affected children (a 13-year-old girl and her 7- and 8-year-old brothers) in a sibship of eight had findings consistent with the Saldino-Mainzer syndrome (skeletal dysplasia associated with Leber's congenital amaurosis, familial juvenile nephronophthisis, and cone-shaped epiphyses of the hands). Two also had pigmented midline nevi. Although tapetoretinal degeneration and familial juvenile nephronophthisis are associated in the inherited Senior-Loken syndrome, the rare association of these abnormalities with cone-shaped epiphyses of the hands suggested an autosomal recessive syndrome with variable expression remarkably similar to the Saldino-Mainzer syndrome, which may or may not be distinct from the Senior-Loken syndrome. The association of tapetoretinal degeneration with skeletal dysplasia may indicate asymptomatic renal or hepatic disease.

Entities:  

Mesh:

Year:  1984        PMID: 6696034     DOI: 10.1016/s0002-9394(14)76095-7

Source DB:  PubMed          Journal:  Am J Ophthalmol        ISSN: 0002-9394            Impact factor:   5.258


  9 in total

1.  A novel locus for Leber congenital amaurosis maps to chromosome 6q.

Authors:  S Dharmaraj; Y Li; J M Robitaille; E Silva; D Zhu; T N Mitchell; L P Maltby; A B Baffoe-Bonnie; I H Maumenee
Journal:  Am J Hum Genet       Date:  2000-01       Impact factor: 11.025

2.  Nephronophthisis.

Authors:  Roslyn J Simms; Lorraine Eley; John A Sayer
Journal:  Eur J Hum Genet       Date:  2008-12-10       Impact factor: 4.246

3.  A new oculorenal syndrome: retinal dystrophy and tubulointerstitial nephropathy in cranioectodermal dysplasia.

Authors:  T Eke; G Woodruff; I D Young
Journal:  Br J Ophthalmol       Date:  1996-05       Impact factor: 4.638

4.  Leber's congenital amaurosis--a new syndrome with a cardiomyopathy.

Authors:  I M Russell-Eggitt; D S Taylor; P T Clayton; A Garner; A Kriss; J F Taylor
Journal:  Br J Ophthalmol       Date:  1989-04       Impact factor: 4.638

5.  Senior-Løken syndrome with marbelized fundus and unusual skeletal abnormalities. A case report.

Authors:  B Lauweryns; A Leys; E Van Haesendonck; L Missotten
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1993-04       Impact factor: 3.117

Review 6.  Nephronophthisis.

Authors:  Matthias T F Wolf; Friedhelm Hildebrandt
Journal:  Pediatr Nephrol       Date:  2010-07-22       Impact factor: 3.714

7.  Hereditary renal and retinal dysplasia--the Senior-Loken syndrome.

Authors:  A H Bell; P J McKiernen; J M Savage; M M Reid
Journal:  Ulster Med J       Date:  1987-10

Review 8.  Many Genes-One Disease? Genetics of Nephronophthisis (NPHP) and NPHP-Associated Disorders.

Authors:  Shalabh Srivastava; Elisa Molinari; Shreya Raman; John A Sayer
Journal:  Front Pediatr       Date:  2018-01-05       Impact factor: 3.418

9.  Wide-spread cone-shaped epiphyses in two Saudi siblings with Ellis-van Creveld syndrome.

Authors:  Abeer Al-Fardan; Mohammad M Al-Qattan
Journal:  Int J Surg Case Rep       Date:  2017-08-24
  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.