Cargando…

Renal transplantation in a patient with Bartter syndrome and glomerulosclerosis

Bartter syndrome (BS) is a clinically and genetically heterogeneous inherited renal tube disorder characterized by renal salt wasting, hypokalemic metabolic alkalosis and normotensive hyperreninemic hyperaldosteronism. There have been several case reports of BS complicated by focal segmental glomeru...

Descripción completa

Detalles Bibliográficos
Autores principales:	Lee, Se Eun, Han, Kyoung Hee, Jung, Yun Hye, Lee, Hyun Kyung, Kang, Hee Gyung, Moon, Kyung Chul, Ha, Il Soo, Choi, Yong, Cheong, Hae Il
Formato:	Texto
Lenguaje:	English
Publicado:	The Korean Pediatric Society 2011
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3040364/ https://www.ncbi.nlm.nih.gov/pubmed/21359059 http://dx.doi.org/10.3345/kjp.2011.54.1.36

Ejemplares similares

A case of Bartter syndrome type I with atypical presentations
por: Lee, Eun Hye, et al.
Publicado: (2010)

Bilateral iliac and popliteal arterial thrombosis in a child with focal segmental glomerulosclerosis
por: Han, Kyoung Hee, et al.
Publicado: (2016)

Recurrence and Treatment after Renal Transplantation in Children with FSGS
por: Kang, Hee Gyung, et al.
Publicado: (2016)

A case of pseudohypoaldosteronism type 1 with a mutation in the mineralocorticoid receptor gene
por: Lee, Se Eun, et al.
Publicado: (2011)

Translational Read-Through of a Nonsense Mutation Causing Bartter Syndrome
por: Cho, Hee Yeon, et al.
Publicado: (2013)

Long-term outcome of Bartter syndrome in 54 patients: A multicenter study in Korea
por: Choi, Naye, et al.
Publicado: (2023)

Corrigendum: Long-term outcome of Bartter syndrome in 54 patients: a multicenter study in Korea
por: Choi, Naye, et al.
Publicado: (2023)

A novel mutation of CLCNKB in a Korean patient of mixed phenotype of Bartter-Gitelman syndrome
por: Cho, Hee-Won, et al.
Publicado: (2016)

A nonsense PAX6 mutation in a family with congenital aniridia
por: Han, Kyoung Hee, et al.
Publicado: (2016)

Bartter Syndrome: Perspectives of a Pediatric Nephrologist
por: Choi, Naye, et al.
Publicado: (2022)

Disseminated adenovirus infection in a 10-year-old renal allograft recipient
por: Lee, Bora, et al.
Publicado: (2018)

A Pediatric Case of a D-Penicillamine Induced ANCA-associated Vasculitis Manifesting a Pulmonary-Renal Syndrome
por: Kang, Sena, et al.
Publicado: (2019)

Genetic Study in Korean Pediatric Patients with Steroid-Resistant Nephrotic Syndrome or Focal Segmental Glomerulosclerosis
por: Park, Eujin, et al.
Publicado: (2020)

Autosomal dominant hypocalcemia with Bartter syndrome due to a novel activating mutation of calcium sensing receptor, Y829C
por: Choi, Keun Hee, et al.
Publicado: (2015)

Higher Incidence of BK Virus Nephropathy in Pediatric Kidney Allograft Recipients with Alport Syndrome
por: Cho, Young Hoon, et al.
Publicado: (2019)

Acute kidney injury associated with Yersinia pseudotuberculosis infection: Forgotten but not gone
por: Kim, Ye Kyung, et al.
Publicado: (2019)

Renal Syndromic Hearing Loss Is Common in Childhood-onset Chronic Kidney Disease
por: Kim, Ji Hyun, et al.
Publicado: (2020)

Reninoma: a rare cause of curable hypertension
por: Kim, Ji Hye, et al.
Publicado: (2019)

Outcomes of chronic dialysis in Korean children with respect to survival rates and causes of death
por: Chang, Hye Jin, et al.
Publicado: (2014)

Two Korean Infants with Genetically Confirmed Congenital Nephrotic Syndrome of Finnish Type
por: Lee, Beom Hee, et al.
Publicado: (2009)

Kidney Transplantation in Patients with Atypical Hemolytic Uremic Syndrome due to Complement Factor H Deficiency: Impact of Liver Transplantation
por: Kim, Sejin, et al.
Publicado: (2017)

Survival over 2 years of autosomal-recessive renal tubular dysgenesis
por: Kim, Su Yeong, et al.
Publicado: (2012)

A Premature Baby with Severe Oligohydramnios and Hypotension: a Case Report of Renal Tubular Dysgenesis
por: Min, Jeesu, et al.
Publicado: (2020)

Correction: Park et al. Genetic Study in Korean Pediatric Patients with Steroid-Resistant Nephrotic Syndrome or Focal Segmental Glomerulosclerosis. J. Clin. Med. 2020, 9, 2013
por: Park, Eujin, et al.
Publicado: (2022)

Genotype and Phenotype Analyses in Pediatric Patients with HNF1B Mutations
por: Lim, Seon Hee, et al.
Publicado: (2020)

Post-Transplant Lymphoproliferative Diseases in Pediatric Kidney Allograft Recipients with Epstein-Barr Virus Viremia
por: Hyun, Hyesun, et al.
Publicado: (2019)

Erratum: Post-Transplant Lymphoproliferative Diseases in Pediatric Kidney Allograft Recipients with Epstein-Barr Virus Viremia
por: Hyun, Hyesun, et al.
Publicado: (2020)

Measurement of Fluid Status Using Bioimpedance Methods in Korean Pediatric Patients on Hemodialysis
por: Yang, Eun Mi, et al.
Publicado: (2017)

Outcome of Antimicrobial Therapy of Pediatric Urinary Tract Infections Caused by Extended-Spectrum β-Lactamase-Producing Enterobacteriaceae
por: Lee, Bongjin, et al.
Publicado: (2013)

Mechanism of Chronic Kidney Disease Progression and Novel Biomarkers: A Metabolomic Analysis of Experimental Glomerulonephritis
por: Han, Kyoung Hee, et al.
Publicado: (2020)

Genotype and Phenotype Analysis in X-Linked Hypophosphatemia
por: Park, Peong Gang, et al.
Publicado: (2021)

Association between Serum Matrix Metalloproteinase- (MMP-) 3 Levels and Systemic Lupus Erythematosus: A Meta-analysis
por: Lee, Jiwon M., et al.
Publicado: (2019)

Corrigendum to “Association between Serum Matrix Metalloproteinase- (MMP-) 3 Levels and Systemic Lupus Erythematosus: A Meta-Analysis”
por: Lee, Jiwon M., et al.
Publicado: (2020)

Amyloid light-chain amyloidosis presented as focal segmental glomerulosclerosis in a kidney transplant recipient
por: Park, Sung Hyun, et al.
Publicado: (2020)

Genotype and Phenotype Analysis in Pediatric Patients with Cystinuria
por: Kim, Ji Hyun, et al.
Publicado: (2017)

Long-term repeated rituximab treatment for childhood steroid-dependent nephrotic syndrome
por: Kim, Ji Hyun, et al.
Publicado: (2017)

KNOW-Ped CKD (KoreaN cohort study for outcomes in patients with pediatric CKD): Design and methods
por: Kang, Hee Gyung, et al.
Publicado: (2016)

Clinico-Genetic Study of Nail-Patella Syndrome
por: Lee, Beom Hee, et al.
Publicado: (2009)

Nephrotic syndrome: what's new, what's hot?
por: Kang, Hee Gyung, et al.
Publicado: (2015)

Effects of pretransplant plasmapheresis and rituximab on recurrence of focal segmental glomerulosclerosis in adult renal transplant recipients
por: Park, Hoon Suk, et al.
Publicado: (2014)

Cannot write session to /tmp/vufind_sessions/sess_ujdl0ag2odnv87v777382jsffm