Cargando…

The Challenges of Diagnosing and Following Wilson Disease in the Presence of Proteinuria

The coexistence of Wilson disease with Alport syndrome has not previously been reported. The diagnosis of Wilson disease and its ongoing monitoring is challenging when associated with an underlying renal disease such as Alport syndrome. Proteinuria can lead to low ceruloplasmin since it is among ser...

Descripción completa

Detalles Bibliográficos
Autores principales:	Khan, Soofia, Schilsky, Michael, Silber, Gary, Morgenstern, Bruce, Miloh, Tamir
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition 2016
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4942312/ https://www.ncbi.nlm.nih.gov/pubmed/27437191 http://dx.doi.org/10.5223/pghn.2016.19.2.139

Ejemplares similares

Trientine induced colitis during therapy for Wilson disease: a case report and review of the literature
por: Boga, Salih, et al.
Publicado: (2015)

Presentation of Progressive Familial Intrahepatic Cholestasis Type 3 Mimicking Wilson Disease: Molecular Genetic Diagnosis and Response to Treatment
por: Boga, Salih, et al.
Publicado: (2015)

Wilson’s Disease: Facing the Challenge of Diagnosing a Rare Disease
por: Sánchez-Monteagudo, Ana, et al.
Publicado: (2021)

Prospective Pilot Study of a Single Daily Dosage of Trientine for the Treatment of Wilson Disease
por: Ala, Aftab, et al.
Publicado: (2015)

A Case for Not Going Global: “Americanization” of Diet Accelerates Hepatic Mitochondrial Injury in a Model of Wilson Disease
por: To, Uyen, et al.
Publicado: (2019)

Designing Clinical Trials in Wilson’s Disease
por: Ott, Peter, et al.
Publicado: (2021)

Zinc Maintenance Therapy for Wilson Disease: A Comparison Between Zinc Acetate and Alternative Zinc Preparations
por: Camarata, Michelle A., et al.
Publicado: (2019)

Challenges with neuropsychiatric Wilson's disease
por: Åberg, Fredrik, et al.
Publicado: (2023)

The dilemma to diagnose Wilson disease by genetic testing alone
por: Stättermayer, Albert Friedrich, et al.
Publicado: (2019)

Oral Vancomycin Therapy in a Child with Primary Sclerosing Cholangitis and Severe Ulcerative Colitis
por: Buness, Cynthia, et al.
Publicado: (2016)

Wilson's Disease: Diagnosis of Wilson's Disease in Ethiopian Young Sisters
por: Bekele, Nebiyu, et al.
Publicado: (2020)

Wilson disease – Challenge for safe anesthesia!
por: Kaur, Arminder, et al.
Publicado: (2019)

A Challenging Case of Wilson's Disease
por: João Soares, Rita, et al.
Publicado: (2023)

Clinically diagnosed late-onset fulminant Wilson’s disease without cirrhosis: A case report
por: Amano, Takahiro, et al.
Publicado: (2018)

Challenges and dilemmas in pediatric hepatic Wilson’s disease
por: Ghosh, Upasana, et al.
Publicado: (2023)

Blink reflex in newly diagnosed and treated patients with Wilson’s disease
por: Bembenek, Jan P., et al.
Publicado: (2021)

Undulating tongue in Wilson's disease
por: Nagappa, M, et al.
Publicado: (2014)

HSD17B13 truncated variant is associated with a mild hepatic phenotype in Wilson’s Disease
por: Ferenci, Peter, et al.
Publicado: (2019)

Wilson disease diagnosed incidentally by targeted gene panel sequencing in a Korean boy with severe obesity
por: Im, Minji, et al.
Publicado: (2022)

Isolated proteinuria due to CUBN homozygous mutation – challenging the investigative paradigm
por: Jayasinghe, Kushani, et al.
Publicado: (2019)

Characteristics of a newly diagnosed Polish cohort of patients with neurological manifestations of Wilson disease evaluated with the Unified Wilson’s Disease Rating Scale
por: Członkowska, Anna, et al.
Publicado: (2018)

Sleep disturbances in newly diagnosed treatment-naïve patients with Wilson’s disease
por: Jernajczyk, Wojciech, et al.
Publicado: (2022)

Lysinuric protein intolerance in a family of Mexican ancestry with a novel SLC7A7 gene deletion. Case report and review of the literature
por: Carpentieri, David, et al.
Publicado: (2015)

Wilson's Disease : A Case Report
por: Shah, Hemang, et al.
Publicado: (2003)

Severe neuropsychiatric presentation of Wilson's disease
por: Chakor, Rahul T., et al.
Publicado: (2011)

Wilson's disease masquerading as nonalcoholic steatohepatitis
por: Mahmood, Sabina, et al.
Publicado: (2009)

Mismanagement of Wilson's disease as psychotic disorder
por: Bidaki, Reza, et al.
Publicado: (2012)

Isolated lingual involvement in Wilson's disease
por: Choudhary, Neera, et al.
Publicado: (2015)

Wilson’s Disease Presenting as Resistant Rickets
por: Goyal, Jagdish P, et al.
Publicado: (2011)

Practical challenges of diagnosing obstruction in the presence of restriction
por: Neder, José Alberto, et al.
Publicado: (2019)

Cystatin C as a surrogate for glomerular filtration rate in the presence of proteinuria
por: Ledson, Thomas, et al.
Publicado: (2008)

Anemia following zinc treatment for Wilson’s disease: a case report and literature review
por: Cai, Sha, et al.
Publicado: (2019)

Wilson's Disease
por: Glazebrook, A. J.
Publicado: (1945)

Wilson's Disease
por: Vukasovic, Ines
Publicado: (2004)

Wilson France: a national database for Wilson’s disease
por: Trocello, Jean-Marc
Publicado: (2010)

Antihypertensive treatment and risk of cardiovascular mortality in patients with chronic kidney disease diagnosed based on the presence of proteinuria and renal function: A large longitudinal study in Japan
por: Nagai, Kei, et al.
Publicado: (2019)

WILSON'S DISEASE PRESENTING WITH OBSESSIVE-COMPULSIVE DISORDER
por: Duggal, Harpreet S., et al.
Publicado: (2000)

Endocrine Symptoms as the Initial Manifestation of Wilson’s Disease
por: Krysiak, Robert, et al.
Publicado: (2012)

Generalized hyperpigmentation in Wilson's disease: An unusual association
por: Nandi, Madhumita, et al.
Publicado: (2013)

Acute-Onset Optic Neuropathy in Wilson's Disease
por: Chou, Liyung Tiffany, et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_4mdl180o6vuevs9q3su32jrocj