Cargando…

A Late Presentation of a Fatal Disease: Juvenile Hemochromatosis

Juvenile hemochromatosis is a rare and severe form of hereditary hemochromatosis. We report the case of a 39-year-old female who presented with heart failure and cirrhosis from previously unrecognized juvenile hemochromatosis. This is the latest presentation described in the literature. An important...

Descripción completa

Detalles Bibliográficos
Autores principales:	Cherfane, Cynthia, Lee, Pauline, Guerin, Leana, Brown, Kyle
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Hindawi Publishing Corporation 2013
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3784272/ https://www.ncbi.nlm.nih.gov/pubmed/24106505 http://dx.doi.org/10.1155/2013/875093

Ejemplares similares

Juvenile Hemochromatosis in an Asymptomatic Patient—Importance of Early Diagnosis
por: Nashed, Bola, et al.
Publicado: (2022)

Juvenile Hemochromatosis due to a Homozygous Variant in the HJV Gene
por: Moreno-Risco, María-Belén, et al.
Publicado: (2022)

Hemochromatosis as Junctional Tachycardia, a Rare Presentation
por: Ghani, Ali, et al.
Publicado: (2017)

Severe osteoporosis as atypical presentation of hereditary hemochromatosis
por: Taujan, Georgiana Cristina, et al.
Publicado: (2022)

A Rare Presentation of Transfusional Hemochromatosis: Hypogonadotropic Hypogonadism
por: Ucler, Rifki, et al.
Publicado: (2015)

Juvenile hemochromatosis: HAMP mutation and severe iron overload treated with phlebotomies and deferasirox
por: Lescano, Manuel A, et al.
Publicado: (2017)

Late-onset Hemochromatosis: Co-inheritance of β-thalassemia and Hereditary Hemochromatosis in a Chinese Family: A Case Report and Epidemiological Analysis of Diverse Populations
por: Yang, Jinjun, et al.
Publicado: (2017)

Clinicopathological diagnosis and treatment of juvenile hemochromatosis
por: Li, Chun-Xing, et al.
Publicado: (2019)

Juvenile Hemochromatosis in Iran: A Case Report with 5-Year Follow-up after Treatment
por: Nobakht, Hossein, et al.
Publicado: (2016)

Reversal of end-stage heart failure in juvenile hemochromatosis with iron chelation therapy: a case report
por: Cooray, Shamil D., et al.
Publicado: (2018)

Primary hemochromatosis presented by porphyria cutanea tarda: a case report
por: Bovenschen, H Jorn, et al.
Publicado: (2009)

Juvenile Hemochromatosis: A Case Report and Review of the Literature
por: Takami, Akiyoshi, et al.
Publicado: (2020)

Levodopa Responsive Parkinsonism in Patients with Hemochromatosis: Case Presentation and Literature Review
por: Girotra, Tarun, et al.
Publicado: (2017)

Neonatal Lupus presenting with neonatal hemochromatosis-like liver disease that responded to steroids: a case report
por: Khayat, Ammar Abdulaziz, et al.
Publicado: (2022)

Inflammation can increase hepcidin in HFE‐hereditary hemochromatosis
por: Moris, Wenke, et al.
Publicado: (2021)

Hypoparathyroidism and Subclinical Hypothyroidism with Secondary Hemochromatosis
por: Jeong, Hyung Ki, et al.
Publicado: (2014)

Primary Hemochromatosis Presenting as Type 2 Diabetes Mellitus: A Case Report with Review of Literature
por: Raju, Kalyani, et al.
Publicado: (2018)

An unfortunate case of acquired hemochromatosis: a case report review of the clinical presentation, diagnosis, management, and prognosis
por: Tariq, Anam, et al.
Publicado: (2016)

Early presentation of adult-onset conditions: A dual diagnosis of hereditary hemochromatosis and porphyria cutanea tarda
por: Strong, Alanna, et al.
Publicado: (2020)

Idiopathic brain calcification in a patient with hereditary hemochromatosis
por: Scarlini, Stefania, et al.
Publicado: (2020)

Metastatic breast cancer presenting as acute liver injury: diagnostic dilemma in the setting of suspected hemochromatosis
por: Chandradevan, Raguraj, et al.
Publicado: (2020)

Bull's eye maculopathy associated with hereditary hemochromatosis
por: Bellsmith, Kellyn N., et al.
Publicado: (2020)

Clinical burden of liver disease from hemochromatosis at an academic medical center
por: Sánchez‐Luna, Sergio A., et al.
Publicado: (2017)

Juvenile Hemochromatosis: Rheumatic Manifestations of 2 Sisters Responding to Deferasirox Treatment. A Case Series and Literature Review
por: Alqanatish, Jubran, et al.
Publicado: (2021)

Late‐onset argininosuccinic aciduria in a 72‐year‐old man presenting with fatal hyperammonemia
por: Leuger, Laurent, et al.
Publicado: (2021)

A liver fibrosis cocktail? Psoriasis, methotrexate and genetic hemochromatosis
por: Mathew, Joseph, et al.
Publicado: (2005)

Hemochromatosis, alcoholism and unhealthy dietary fat: a case report
por: Shobi, Venkatachalam, et al.
Publicado: (2021)

Clinical and Imaging Resolution of Neonatal Hemochromatosis following Treatment
por: Machtei, Ayelet, et al.
Publicado: (2014)

Secondary Hemochromatosis due to Chronic Oral Iron Supplementation
por: Lands, Ronald, et al.
Publicado: (2017)

Living Related Liver Transplantation in an Infant with Neonatal Hemochromatosis
por: Choi, Shin Jie, et al.
Publicado: (2016)

Hereditary hemochromatosis and JAK2‐positive polycythemia vera
por: Radwan, Ahmed, et al.
Publicado: (2021)

Disseminated cryptococcosis and hemochromatosis: clues to diagnosis
por: Nichols, Larry, et al.
Publicado: (2020)

Heterogeneous Presentation of Neonatal Hemochromatosis in Dichorionic Twins
por: Chee, Yee Yuet, et al.
Publicado: (2018)

Fatal refractory cardiac arrest as presentation of systemic amyloidosis
por: Chung, Peter, et al.
Publicado: (2020)

Successful treatment of hemochromatosis with renal tubular dysgenesis in a preterm infant
por: Koura, Uta, et al.
Publicado: (2015)

Hepatocellular Carcinoma Arising in a Non-cirrhotic Liver with Secondary Hemochromatosis
por: Yamauchi, Ryo, et al.
Publicado: (2018)

Juvenile Hemochromatosis, Genetic Study and Long-term Follow up after Therapy
por: Malekzadeh, Masoud M., et al.
Publicado: (2014)

Sporadic Porphyria Cutanea Tarda as the Initial Manifestation of Hereditary Hemochromatosis
por: Edwards, Mitchell V., et al.
Publicado: (2019)

Iron Man: Non-HFE Hemochromatosis Without Significant Fibrosis
por: Chaudhry, Hunza, et al.
Publicado: (2023)

A fatal case of seronegative, late-onset systemic lupus erythematosus presenting with motor sensory axonal polyneuropathy
por: Anyfantakis, Dimitrios, et al.
Publicado: (2013)

Cannot write session to /tmp/vufind_sessions/sess_88jgd9ka59j0n6ekshdah09anb