Literature DB >> 7362813

Sector retinitis pigmentosa in juvenile nephronophthisis.

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

Abstract

In a patient with juvenile nephronophthisis, sector retinitis pigmentosa was found as an extrarenal manifestation, establishing a hitherto undescribed variety of retinal degeneration occurring in this disorder. The retinal function in this case was identical with that in the classic type of sector retinitis pigmentosa, namely, subnormal ERG amplitudes but normal cone and rod implicit times. The range of the retinal findings and their autosomal recessive transmission are discussed. Paucity of information makes it difficult to elucidate the basic genetic defect operating in this condition.

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Year:  1980        PMID: 7362813      PMCID: PMC1039362          DOI: 10.1136/bjo.64.2.124

Source DB:  PubMed          Journal:  Br J Ophthalmol        ISSN: 0007-1161            Impact factor:   4.638


  13 in total

1.  Tapetoretinal degeneration associated with recessively inherited medullary cystic disease.

Authors:  B C Polak; B L Hogewind; F H Van Lith
Journal:  Am J Ophthalmol       Date:  1977-11       Impact factor: 5.258

2.  Congenital hepatic fibrosis and nephronophthisis. A family study.

Authors:  H Boichis; J Passwell; R David; H Miller
Journal:  Q J Med       Date:  1973-01

3.  Temporal aspects of the electroretinogram in sector retinitis pigmentosa.

Authors:  E L Berson; J Howard
Journal:  Arch Ophthalmol       Date:  1971-12

4.  Familial juvenile nephronophthisis and medullary cystic disease.

Authors:  F A Pedreira; E L Marmer; W H Bergstrom
Journal:  J Pediatr       Date:  1968-07       Impact factor: 4.406

5.  Medullary cystic disease with macular degeneration.

Authors:  J D Price; J A Pratt-johnson
Journal:  Can Med Assoc J       Date:  1970-01       Impact factor: 8.262

6.  Sector retinitis pigmentosa.

Authors:  A E Krill; D Archer; D Martin
Journal:  Am J Ophthalmol       Date:  1970-06       Impact factor: 5.258

7.  Hereditary renal-retinal dysplasia.

Authors:  R N Schimke
Journal:  Ann Intern Med       Date:  1969-04       Impact factor: 25.391

8.  Congenital amaurosis and nephrophthisis: a new syndrome.

Authors:  I E Hussels
Journal:  Birth Defects Orig Artic Ser       Date:  1971-03

9.  Familial nephropathy associatdd with retinitis pigmentosa, cerebellar ataxia and skeletal abnormalities.

Authors:  F Mainzer; R M Saldino; M B Ozonoff; H Minagi
Journal:  Am J Med       Date:  1970-10       Impact factor: 4.965

10.  Nephronophthisis and medullary cystic disease.

Authors:  J G Mongeau; H G Worthen
Journal:  Am J Med       Date:  1967-09       Impact factor: 4.965

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  4 in total

1.  Senior-Loken syndrome. Case reports of two siblings and association with sensorineural deafness.

Authors:  M P Clarke; T J Sullivan; C Francis; R Baumal; T Fenton; W G Pearce
Journal:  Br J Ophthalmol       Date:  1992-03       Impact factor: 4.638

2.  Atypical sector pigmentary dystrophy.

Authors:  A Pinckers; J Greydanus; A F Deutman; K U Duinkerke-Eerola
Journal:  Int Ophthalmol       Date:  1986-05       Impact factor: 2.031

3.  Senior-loken syndrome with rare manifestations: a case report.

Authors:  Harikrishan K Aggarwal; Deepak Jain; Sachin Yadav; Vipin Kaverappa; Abhishek Gupta
Journal:  Eurasian J Med       Date:  2013-06

4.  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 in total

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