Literature DB >> 3284122

Nephropathy of nail-patella syndrome.

T Taguchi1, S Takebayashi, M Nishimura, N Tsuru.   

Abstract

Ultrastructural renal lesions of a sporadic case of nail-patella syndrome are described. Although the patient, an 8-year-old Japanese boy, had no clinical renal syndrome, electron microscopy disclosed the presence of collagen fibrils and electron lucent areas within glomerular basement membrane. Comparative observation of glomeruli in sections stained by uranyl-acetate and lead-citrate and those by PTAH-uranyl revealed evidence of many collagen fibrils in mesangial matrix, as well as glomerular basement membrane. At the follow-up study 3 years after the biopsy, he still showed normal urinalysis and no renal dysfunction. Characteristic ultrastructure of glomerulus of this disease can be present even in cases without any apparent clinical renal involvement. It is concluded that the glomerular lesions in nail-patella syndrome may be caused by abnormal metabolic processes of collagen in glomeruli rather than entrapment of circulating collagen precursors.

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Year:  1988        PMID: 3284122     DOI: 10.3109/01913128809058216

Source DB:  PubMed          Journal:  Ultrastruct Pathol        ISSN: 0191-3123            Impact factor:   1.094


  6 in total

1.  Unusual glomerulopathy with atypical thickening of the glomerular basement membrane and intramembranous microparticles.

Authors:  Arifa Nazneen; Yumoko Nakashima; Yan Zha; Viet Thang Le; Takashi Taguchi; Katsuaki Nishioka; Masato Tadokoro; Koichi Taura
Journal:  Clin Exp Nephrol       Date:  2008-11-18       Impact factor: 2.801

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.  Familial glomerulopathy with proximal tubular dysfunction: a new syndrome?

Authors:  T K Mattoo; M Akhtar
Journal:  Pediatr Nephrol       Date:  1990-05       Impact factor: 3.714

4.  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

5.  In vivo expression of putative LMX1B targets in nail-patella syndrome kidneys.

Authors:  Laurence Heidet; Ernie M H F Bongers; Mireille Sich; Shao-Yu Zhang; Chantal Loirat; Alain Meyrier; Michel Broyer; Gérard Landthaler; Bernadette Faller; Yoshikazu Sado; Nine V A M Knoers; Marie-Claire Gubler
Journal:  Am J Pathol       Date:  2003-07       Impact factor: 4.307

6.  Clinico-genetic study of nail-patella syndrome.

Authors:  Beom Hee Lee; Tae-Joon Cho; Hyun Jin Choi; Hee Kyung Kang; In Seok Lim; Yong-Hoon Park; Il Soo Ha; Yong Choi; Hae Il Cheong
Journal:  J Korean Med Sci       Date:  2009-01-28       Impact factor: 2.153

  6 in total

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