Literature DB >> 1149338

Nephronophthisis and tapetoretinal degeneration associated with liver fibrosis.

W Proesmans, B Van Damme, J Macken.   

Abstract

A 12 year-old boy was referred because of general weakness, enuresis and pallor which had been present for at least six months. Previously, the child had been hospitalized at the age of five, because of mental retardation and hepatosplenomegaly, for which no cause could be found. He had severe renal insufficiency, with all the hallmarks of nephronophthisis. In addition his vision was very poor and fundoscopy revealed tapetoretinal degeneration. The liver and spleen were grossly enlarged. Liver function was almost completely normal, but histology showed diffuse periportal febrosis with profiferation of the bile ducts. This observation seems to confirm the existence of a new syndrome, associating nephronophthisis and liver fibrosis as described by Boichis and coworkers (1973).

Entities:  

Mesh:

Year:  1975        PMID: 1149338

Source DB:  PubMed          Journal:  Clin Nephrol        ISSN: 0301-0430            Impact factor:   0.975


  13 in total

1.  Nephronophthisis.

Authors:  W Proesmans; B van Damme
Journal:  Arch Dis Child       Date:  1977-06       Impact factor: 3.791

2.  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

3.  The nephronophthisis complex. A clinicopathologic study in children.

Authors:  R Waldherr; T Lennert; H P Weber; H J Födisch; K Schärer
Journal:  Virchows Arch A Pathol Anat Histol       Date:  1982

Review 4.  Progressive tubulointerstitial nephropathy with hepatic involvement in an infant.

Authors:  B Henrot; C Vermylen; D Caus; J P Cosyns; S Gosseye; G Verellen; G Cornu
Journal:  Eur J Pediatr       Date:  1990-02       Impact factor: 3.183

5.  Infantile chronic tubulo-interstitial nephritis with cortical microcysts: variant of nephronophthisis or new disease entity?

Authors:  M F Gagnadoux; J L Bacri; M Broyer; R Habib
Journal:  Pediatr Nephrol       Date:  1989-01       Impact factor: 3.714

6.  Familial juvenile nephronophthisis, Jeune's syndrome, and associated disorders.

Authors:  M D Donaldson; A A Warner; R S Trompeter; G B Haycock; C Chantler
Journal:  Arch Dis Child       Date:  1985-05       Impact factor: 3.791

Review 7.  Progressive tubulointerstitial nephritis and chronic cholestatic liver disease.

Authors:  M Popović-Rolović; M Kostić; M Sindjić; O Jovanović; A Peco-Antić; D Kruscić
Journal:  Pediatr Nephrol       Date:  1993-08       Impact factor: 3.714

Review 8.  The nephronophthisis complex: clinical and genetic aspects.

Authors:  F Hildebrandt; R Waldherr; R Kutt; M Brandis
Journal:  Clin Investig       Date:  1992-09

9.  Hereditary renal-retinal dysplasia.

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

10.  Ocular changes in some progressive hereditary nephropathies.

Authors:  J L Dufier; D Orssaud; P Dhermy; M C Gubler; M F Gagnadoux; C Kleinknecht; M Broyer
Journal:  Pediatr Nephrol       Date:  1987-07       Impact factor: 3.714

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