نتایج جستجو برای: alport syndrome

تعداد نتایج: 622022  

2014
Jeffrey H. Miner

Malone et al. performed next-generation sequencing on 70 families with focal segmental glomerulosclerosis (FSGS) and discovered that 10% had variants in surprising 'old' genes, COL4A3 and COL4A4, which are involved in Alport syndrome and thin basement membrane nephropathy. These data show that a subset of renal manifestations associated with COL4A3 or COL4A4 variants cannot be distinguished fro...

2016
Tomohiro Murata Kan Katayama Toshitaka Oohashi Timo Jahnukainen Tomoko Yonezawa Yoshikazu Sado Eiji Ishikawa Shinsuke Nomura Karl Tryggvason Masaaki Ito

Alport syndrome is caused by mutations in the genes encoding α3, α4, or α5 (IV) chains. Unlike X-linked Alport mice, α5 and α6 (IV) chains are detected in the glomerular basement membrane of autosomal recessive Alport mice, however, the significance of this finding remains to be investigated. We therefore generated mice lacking both α3 and α6 (IV) chains and compared their renal function and su...

Journal: :PLoS Medicine 2006
Michael Zeisberg Mona Khurana Velidi H Rao Dominic Cosgrove Jean-Philippe Rougier Michelle C Werner Charles F Shield Zena Werb Raghu Kalluri

BACKGROUND Glomerular basement membrane (GBM), a key component of the blood-filtration apparatus in the in the kidney, is formed through assembly of type IV collagen with laminins, nidogen, and sulfated proteoglycans. Mutations or deletions involving alpha3(IV), alpha4(IV), or alpha5(IV) chains of type IV collagen in the GBM have been identified as the cause for Alport syndrome in humans, a pro...

Journal: :Hippokratia 2008
E Lagona L Tsartsali S Kostaridou A Skiathitou E Georgaki F Sotsiou

Alport syndrome (AS) is the most common hereditary nephritis often associated with extrarenal manifestations. It was first described by Alport on 1927. There is a primary disorder in collagen type IV which is the main component of the basement membranes. Alport syndrome is more frequently inherited as an X-linked and less commonly as an autosomal dominant or autosomal recessive trait. We descri...

2012
Wisit Cheungpasitporn Quanhathai Kaewpoowat Promporn Suksaranjit Wonngarm Kittanamongkolchai Narat Srivali

A 19-year-old Caucasian male presented to Nephrology Clinic for evaluation of proteinuria. He denied any hearing or vision impairment. The patient reported significant family history for kidney problem in his father, paternal uncle, paternal aunts and his half brother who shared the same father. Physical examination revealed a blood pressure of 136/60 mmHg with no peripheral edema. Laboratory e...

Journal: :The Journal of clinical investigation 1996
H H Lemmink W N Nillesen T Mochizuki C H Schröder H G Brunner B A van Oost L A Monnens H J Smeets

Benign familial hematuria (BFH) is characterized by autosomal dominant inheritance, thinning of the glomerular basement membrane (GBM) and normal renal function. It is frequent in patients with persistent microscopic hematuria, but cannot be clinically differentiated from the initial stages of Alport syndrome, a severe GBM disorder which progresses to renal failure. We present here linkage of b...

2012
Pilar Antón-Martín Cristina Aparicio López Soraya Ramiro-León Sonia Santillán Garzón Fernando Santos-Simarro Belén Gil-Fournier

BACKGROUND Alport syndrome is a primary basement membrane disorder arising from mutations in genes encoding the type IV collagen protein family. It is a genetically heterogeneous disease with different mutations and forms of inheritance that presents with renal affection, hearing loss and eye defects. Several new mutations related to X-linked forms have been previously determined. METHODS We ...

Journal: :JCI insight 2018
Wen Ding Keyvan Yousefi Stefania Goncalves Bradley J Goldstein Alfonso L Sabater Amy Kloosterboer Portia Ritter Guerline Lambert Armando J Mendez Lina A Shehadeh

Alport syndrome is a rare hereditary renal disorder with no etiologic therapy. We found that osteopontin (OPN) is highly expressed in the renal tubules of the Alport mouse and plays a causative pathological role. OPN genetic deletion ameliorated albuminuria, hypertension, tubulointerstitial proliferation, renal apoptosis, and hearing and visual deficits in the Alport mouse. In Alport renal tubu...

Journal: :Journal of the American Society of Nephrology : JASN 2003
Jean Philippe Jais Bertrand Knebelmann Iannis Giatras Mario De Marchi Gianfranco Rizzoni Alessandra Renieri Manfred Weber Oliver Gross Kai-Olaf Netzer Frances Flinter Yves Pirson Karin Dahan Jörgen Wieslander Ulf Persson Karl Tryggvason Paula Martin Jens Michael Hertz Cornelis Schröder Marek Sanak Maria Fernanda Carvalho Juan Saus Corinne Antignac Hubert Smeets Marie Claire Gubler

Alport syndrome (AS) is a type IV collagen hereditary disease characterized by progressive hematuric nephritis, hearing loss, and ocular changes. Mutations in the COL4A5 collagen gene are responsible for the more common X-linked dominant form of the disease characterized by much less severe disease in girls and women. A "European Community Alport Syndrome Concerted Action" (ECASCA) group was es...

Journal: :Arquivos brasileiros de oftalmologia 2016
Juliana Maria da Silva Rosa Marcelo Vicente de Andrade Sobrinho César Lipener

Alport Syndrome is a hereditary disease that is caused by a gene mutation and affects the production of collagen in basement membranes; this condition causes hemorrhagic nephritis associated with deafness and ocular changes. The X-linked form of this disease is the most common and mainly affects males. Typical ocular findings are dot-and-fleck retinopathy, anterior lenticonus, and posterior pol...

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