Literature DB >> 3351903

Familial spastic paraplegia, bilateral sensorineural deafness, and intellectual retardation associated with a progressive nephropathy.

J S Fitzsimmons1, A R Watson, D Mellor, P R Guilbert.   

Abstract

We present a family in which at least four persons have evidence of an inherited disorder comprising a variable spastic paraplegia, bilateral sensorineural deafness, intellectual retardation, and a progressive nephropathy. Focal segmental proliferative lesions with sclerosis suggestive of mesangial IgA nephropathy (Berger's disease) were found on renal renal biopsy in two affected persons. The glomerular basement membrane showed none of the changes characteristic of Alport's syndrome. Males and females are affected and the segregation of the disease is consistent with dominant transmission.

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Year:  1988        PMID: 3351903      PMCID: PMC1015481          DOI: 10.1136/jmg.25.3.168

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  7 in total

1.  The clinical spectrum of hereditary nephritis.

Authors:  J P Grünfeld
Journal:  Kidney Int       Date:  1985-01       Impact factor: 10.612

Review 2.  Mesangial IgA nephropathy.

Authors:  P Kincaid-Smith; K Nicholls
Journal:  Am J Kidney Dis       Date:  1983-09       Impact factor: 8.860

3.  Alport's syndrome. A report of 58 cases and a review of the literature.

Authors:  M Gubler; M Levy; M Broyer; C Naizot; G Gonzales; D Perrin; R Habib
Journal:  Am J Med       Date:  1981-03       Impact factor: 4.965

4.  Charcot-Marie-Tooth disease and nephritis.

Authors:  G Lemieux; J A Neemeh
Journal:  Can Med Assoc J       Date:  1967-11-11       Impact factor: 8.262

5.  The clinical course of mesangial IgA associated nephropathy in adults.

Authors:  K M Nicholls; K F Fairley; J P Dowling; P Kincaid-Smith
Journal:  Q J Med       Date:  1984

6.  Spastic paresis, glaucoma and mental retardation--a probable autosomal recessive syndrome?

Authors:  G Chenevix-Trench; R Leshner; P Mamunes
Journal:  Clin Genet       Date:  1986-11       Impact factor: 4.438

7.  Hereditary "pure" spastic paraplegia: a clinical and genetic study of 22 families.

Authors:  A E Harding
Journal:  J Neurol Neurosurg Psychiatry       Date:  1981-10       Impact factor: 10.154

  7 in total

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