Literature DB >> 6507504

An autosomal recessive disorder with glomerular basement membrane abnormalities similar to those seen in the nail patella syndrome: report of a kindred.

J R Salcedo.   

Abstract

We present a 9-year-old boy, the product of a consanguineous marriage, with proteinuria, edema, and microscopic hematuria with mild renal impairment since age 2 yr. Renal biopsy showed the histopathologic electron microscopic changes seen in hereditary osteo-onchyodysplasia (HOOD) [Hoyer et al, 1972; Bennet et al, 1973; DelPozo and Lapp 1970; Vernier et al, 1974; Morita et al, 1973] or "nail-patella syndrome." Neither the patient nor his relatives had bone or nail abnormalities; however, 2 other sibs had died of complications of end-stage renal disease at age 6 and 9, leading us to suspect autosomal recessive inheritance of a severe nephropathy or glomerulodysplasia.

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Year:  1984        PMID: 6507504     DOI: 10.1002/ajmg.1320190321

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  9 in total

1.  Two brothers with collagenofibrotic glomerulopathy.

Authors:  Takafumi Aoki; Kazuyuki Hayashi; Takatoshi Morinaga; Hidetaka Tomida; Manabu Hishida; Satoko Yamamoto; Nobuyuki Kajiwara; Hirofumi Tamai
Journal:  CEN Case Rep       Date:  2014-09-18

2.  LMX1B mutations cause hereditary FSGS without extrarenal involvement.

Authors:  Olivia Boyer; Stéphanie Woerner; Fan Yang; Edward J Oakeley; Bolan Linghu; Olivier Gribouval; Marie-Josèphe Tête; José S Duca; Lloyd Klickstein; Amy J Damask; Joseph D Szustakowski; Françoise Heibel; Marie Matignon; Véronique Baudouin; François Chantrel; Jacqueline Champigneulle; Laurent Martin; Patrick Nitschké; Marie-Claire Gubler; Keith J Johnson; Salah-Dine Chibout; Corinne Antignac
Journal:  J Am Soc Nephrol       Date:  2013-05-16       Impact factor: 10.121

3.  Collagen type III glomerulopathy: A case report and review of 20 cases.

Authors:  Junwu Dong; Honglan Wei; Min Han; Yang Guan; Yang Wu; Hua Li
Journal:  Exp Ther Med       Date:  2015-08-20       Impact factor: 2.447

Review 4.  Nail-patella syndrome.

Authors:  Ralph Witzgall
Journal:  Pflugers Arch       Date:  2017-07-05       Impact factor: 3.657

Review 5.  Spectrum of LMX1B mutations: from nail-patella syndrome to isolated nephropathy.

Authors:  Yutaka Harita; Sachiko Kitanaka; Tsuyoshi Isojima; Akira Ashida; Motoshi Hattori
Journal:  Pediatr Nephrol       Date:  2016-07-23       Impact factor: 3.714

6.  Collagen type III glomerulopathy: a new type of hereditary nephropathy.

Authors:  M C Gubler; J P Dommergues; M Foulard; A Bensman; J P Leroy; M Broyer; R Habib
Journal:  Pediatr Nephrol       Date:  1993-08       Impact factor: 3.714

7.  Genetic counselling in hereditary osteo-onychodysplasia (HOOD, nail-patella syndrome) with nephropathy.

Authors:  B J Looij; R L te Slaa; B L Hogewind; J J van de Kamp
Journal:  J Med Genet       Date:  1988-10       Impact factor: 6.318

Review 8.  Genetics of the patella.

Authors:  Mark E Samuels; Philippe M Campeau
Journal:  Eur J Hum Genet       Date:  2019-01-21       Impact factor: 4.246

9.  Nail-patella-like renal disease masquerading as Fabry disease on kidney biopsy: a case report.

Authors:  Filippo Pinto E Vairo; Pavel N Pichurin; Fernando C Fervenza; Samih H Nasr; Kevin Mills; Christopher T Schmitz; Eric W Klee; Sandra M Herrmann
Journal:  BMC Nephrol       Date:  2020-08-13       Impact factor: 2.388

  9 in total

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