Cargando…

High-flow arteriovenous fistula in X-linked Alport syndrome: a case report

Most male X-linked Alport syndrome patients with COL4A5 nonsense mutations experience end-stage kidney failure by 30 years old. Although there is no definition of high-flow arteriovenous fistula, access blood flows greater than 2000 mL/min might predict the occurrence of high-output heart failure. A...

Descripción completa

Detalles Bibliográficos
Autores principales:	Takahashi, Daisuke, Katayama, Kan, Iyoda, Yoshinobu, Fukumori, Ayumi, Tsujimoto, Kayo, Yamawaki, Masahiro, Tanaka, Fumika, Saiki, Ryosuke, Oda, Keiko, Suzuki, Yasuo, Murata, Tomohiro, Okugawa, Yoshinaga, Dohi, Kaoru
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2023
Materias:	Medicine
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10620688/ https://www.ncbi.nlm.nih.gov/pubmed/37928459 http://dx.doi.org/10.3389/fmed.2023.1227283

Ejemplares similares

Three Weeks of Treatment Induced Long-term Remission in a Patient with Micrococcus luteus-related Peritonitis
por: Saiki, Ryosuke, et al.
Publicado: (2022)

Minimal change disease with thrombotic microangiopathy following the Pfizer-BioNTech COVID-19 vaccine
por: Tanaka, Fumika, et al.
Publicado: (2021)

Bullous Pemphigoid in X-linked Alport Syndrome
por: Yamawaki, Masahiro, et al.
Publicado: (2022)

Mother–Son Kidney Transplantation in Patients With X-Linked Alport Syndrome
por: Katayama, Kan, et al.
Publicado: (2021)

A Perihilar Variant of Focal Segmental Glomerulosclerosis Due to De novo Branchio-oto-renal Syndrome
por: Saiki, Ryosuke, et al.
Publicado: (2021)

Membranous nephropathy associated with multicentric Castleman’s disease that was successfully treated with tocilizumab: a case report and review of the literature
por: Saiki, Ryosuke, et al.
Publicado: (2021)

Disruption of the glomerular basement membrane associated with nutcracker syndrome and double inferior vena cava in Noonan syndrome: a case report
por: Omori, Ayumi, et al.
Publicado: (2022)

Mutation Analysis of Autosomal-Dominant Polycystic Kidney Disease Patients
por: Suzuki, Yasuo, et al.
Publicado: (2023)

Recent Advances in Proteinuric Kidney Disease/Nephrotic Syndrome: Lessons from Knockout/Transgenic Mouse Models
por: Saiki, Ryosuke, et al.
Publicado: (2023)

Discordance of light chain isotypes between serum and glomerular deposits in proliferative glomerulonephritis with monoclonal IgG deposits: a case report and review of the literature
por: Miura, Shoko, et al.
Publicado: (2023)

COL4A6 is dispensable for autosomal recessive Alport syndrome
por: Murata, Tomohiro, et al.
Publicado: (2016)

Acute kidney injury due to thin basement membrane disease mimicking Deferasirox nephrotoxicity: a case report
por: Oda, Keiko, et al.
Publicado: (2018)

Granulomatous interstitial nephritis due to chronic lymphocytic leukemia: a case report
por: Suzuki, Yasuo, et al.
Publicado: (2017)

Improvement of Alveolar Hemorrhaging in an Elderly and Renally Impaired Patient with Relapsing Anti-neutrophil Cytoplasmic Autoantibody-associated Vasculitis by Single Infusion of Rituximab
por: Oda, Keiko, et al.
Publicado: (2018)

Biliary peritonitis due to liver cyst rupture in autosomal dominant polycystic kidney disease
por: Matsuo, Hiroshi, et al.
Publicado: (2021)

Mutation Analysis of Thin Basement Membrane Nephropathy
por: Hirabayashi, Yosuke, et al.
Publicado: (2022)

Alport Syndrome With Kidney Cysts Is Still Alport Syndrome
por: Savige, Judy, et al.
Publicado: (2021)

Collagenofibrotic Glomerulopathy
por: Miyake, Masato, et al.
Publicado: (2020)

A Novel Mutation in a Japanese Family with X-linked Alport Syndrome
por: Abe, Yoshifusa, et al.
Publicado: (2016)

Women and Alport syndrome
por: Rheault, Michelle N.
Publicado: (2011)

Alport's Syndrome in Pregnancy
por: Mehta, Suchita, et al.
Publicado: (2013)

Sindrome de Alport : revisión bibliográfica
por: Velasco Bello, Fernando Mario
Publicado: (1994)

Type VI collagen-related nephropathy
por: Mori, Mutsuki, et al.
Publicado: (2022)

Alport syndrome: facts and opinions
por: Kashtan, Clifford
Publicado: (2017)

Genetic diagnosis of Alport syndrome
por: Cheong, Hae Il
Publicado: (2019)

Alport Syndrome Classification and Management
por: Warady, Bradley A., et al.
Publicado: (2020)

Novel Therapies for Alport Syndrome
por: Chavez, Efren, et al.
Publicado: (2022)

Auditory Perception in Alport’s Syndrome
por: Viveiros, Carla Mherlyn, et al.
Publicado: (2015)

Clinical practice recommendations for the treatment of Alport syndrome: a statement of the Alport Syndrome Research Collaborative
por: Kashtan, Clifford E., et al.
Publicado: (2012)

IgM-Positive Tubulointerstitial Nephritis Associated With Asymptomatic Primary Biliary Cirrhosis
por: Mizoguchi, Shoko, et al.
Publicado: (2018)

The 2014 International Workshop on Alport Syndrome
por: Miner, Jeffrey H, et al.
Publicado: (2014)

Anterior lenticonus associated with Alport syndrome
por: Jinagal, Jitender, et al.
Publicado: (2018)

Pulmonary calcinosis associated with Alport syndrome
por: Mismetti, Valentine, et al.
Publicado: (2022)

Alport Syndrome: A Comprehensive Review
por: Adone, Avanti, et al.
Publicado: (2023)

Spontaneous remission of adult-onset minimal change nephrotic syndrome associated with influenza B infection: a case report
por: Haruki, Ayumi, et al.
Publicado: (2018)

A review of clinical characteristics and genetic backgrounds in Alport syndrome
por: Nozu, Kandai, et al.
Publicado: (2018)

Polymorphisms in CPT1B and CPT2 have no significant effect on plasma carnitine levels in Japanese cancer patients
por: Hishida, Asahi, et al.
Publicado: (2019)

Molecular testing for adult type Alport syndrome
por: Pont-Kingdon, Genevieve, et al.
Publicado: (2009)

Podocyte Depletion in Thin GBM and Alport Syndrome
por: Wickman, Larysa, et al.
Publicado: (2016)

It is an Alport syndrome, not a simple hypertensive retinopathy
por: Gadde, Aruna Kumari, et al.
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_6nlo23uhl2dseprma3ctm08vj1