Literature DB >> 1576608

Central nervous system and renal investigations in patients with Lowe syndrome.

S M Pueschel1, A S Brem, P Nittoli.   

Abstract

We describe three patients with Lowe (oculocerebrorenal) syndrome, emphasizing primarily the central nervous system and renal pathology. Using magnetic resonance imaging, we noted diffuse high T2 signals periventricularly, indicating significant white matter destruction, which may be responsible in part for the mental retardation, seizure disorder, hypotonia, and areflexia observed in the patients. In contrast to previously published reports, there was minimal renal tubular dysfunction; however, proteinuria was significantly increased in all patients. We believe that the observed proteinuria is primarily the result of glomerular pathology rather than renal tubular dysfunction and may represent a net loss of negative charges within the glomerular filter. This loss of charge may be linked to the increased excretion of glycosaminoglycans in the urine.

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Year:  1992        PMID: 1576608     DOI: 10.1007/bf00316562

Source DB:  PubMed          Journal:  Childs Nerv Syst        ISSN: 0256-7040            Impact factor:   1.475


  22 in total

1.  Organic-aciduria, decreased renal ammonia production, hydrophthalmos, and mental retardation; a clinical entity.

Authors:  C U LOWE; M TERREY; E A MacLACHLAN
Journal:  AMA Am J Dis Child       Date:  1952-02

2.  Oculocerebrorenal syndrome: case report with CT and MR correlates.

Authors:  L A O'Tuama; D W Laster
Journal:  AJNR Am J Neuroradiol       Date:  1987 May-Jun       Impact factor: 3.825

3.  A defect in intestinal amino acid transport in Lowe's syndrome.

Authors:  C S Bartsocas; H L Levy; J D Crawford; S O Thier
Journal:  Am J Dis Child       Date:  1969-01

4.  Mapping the Lowe oculocerebrorenal syndrome to Xq24-q26 by use of restriction fragment length polymorphisms.

Authors:  D N Silver; R A Lewis; R L Nussbaum
Journal:  J Clin Invest       Date:  1987-01       Impact factor: 14.808

5.  Central nervous system lesions in disorders of amino-acid metabolism. A neuropathological study.

Authors:  J J Martin; W Schlote
Journal:  J Neurol Sci       Date:  1972       Impact factor: 3.181

6.  Mitochondrial defects in Lowe's oculocerebrorenal syndrome.

Authors:  J M Gobernado; M Lousa; A Gimeno; M Gonsalvez
Journal:  Arch Neurol       Date:  1984-02

7.  Urinary acid glycosaminoglycans in a patient with oculo-cerebro-renal syndrome.

Authors:  S Hayashi; T Nagata; A Kimura; K Tsurumi
Journal:  Tohoku J Exp Med       Date:  1978-11       Impact factor: 1.848

8.  Urinary excretion of acid glycosaminoglycans and hydroxyproline in a patient with oculo-cerebro-renal syndrome.

Authors:  S Hayashi; T Nagata; A Kimura; K Tsurumi
Journal:  Tohoku J Exp Med       Date:  1978-11       Impact factor: 1.848

9.  Arthropathy of Lowe's (oculocerebrorenal) syndrome.

Authors:  B H Athreya; H R Schumacher; H D Getz; M E Norman; S Borden; C L Witzleben
Journal:  Arthritis Rheum       Date:  1983-06

10.  MRI findings and peripheral neuropathy in Lowe's syndrome.

Authors:  L Charnas; J Bernar; G H Pezeshkpour; M Dalakas; G S Harper; W A Gahl
Journal:  Neuropediatrics       Date:  1988-02       Impact factor: 1.947

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  3 in total

1.  Neuroimaging and renal ultrasound manifestations of Oculocerebrorenal syndrome of Lowe.

Authors:  Andrew Mark Allmendinger; Naman S Desai; Alanna Teatom Burke; Narayan Viswanadhan; Sanjay Prabhu
Journal:  J Radiol Case Rep       Date:  2014-10-31

Review 2.  The nervous system and chronic kidney disease in children.

Authors:  Debbie S Gipson; Crista E Wetherington; Peter J Duquette; Stephen R Hooper
Journal:  Pediatr Nephrol       Date:  2004-06-18       Impact factor: 3.714

Review 3.  The central nervous system in childhood chronic kidney disease.

Authors:  Debbie S Gipson; Peter J Duquette; Phil F Icard; Stephen R Hooper
Journal:  Pediatr Nephrol       Date:  2006-10-27       Impact factor: 3.714

  3 in total

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