Results 61 to 70 of about 10,302 (227)
Juvenile Hereditary Hemochromatosis: A Case Report [PDF]
Documenta HaematologicaIntroduction: Hereditary hemochromatosis is an inherited condition where an excess of iron is absorbed from the diet, causing its accumulation in vital organs and subsequent organ damage.
Chhavi GOYAL +8 more
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Hepatology Research, EarlyView.ABSTRACT Aim Steatotic liver disease (SLD), including metabolic dysfunction–associated SLD (MASLD) and metabolic dysfunction–associated alcohol‐related liver disease (MetALD), is a growing global health burden. Although impaired mastication is linked to metabolic disorders, its role in SLD remains unclear.
Takashi Miyano +4 more
wiley +1 more source
Hereditary hemochromatosis in the post-HFE era [PDF]
, 2008 Following the discovery of the HFE gene in 1996 and its linkage to the iron overload disorder hereditary hemochromatosis (HH) there have been profound developments in our understanding of the pathogenesis of the biochemical and clinical manifestations of
Olynyk, John K. +13 more
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Hereditary Hemochromatosis: Genetics, Pathogenesis, and Clinical Management
Annals of Hepatology, 2005 Recent findings have led to major advances in our understanding of genetics and pathophysiology of hereditary hemochromatosis. Many crucial genes and molecules have come to light, and the complex interrelationships between them are being studied. However,
Jacob Alexander, Kris V. Kowdley
doaj +1 more source
Case Reports in Oncology, 2020 Infectious mononucleosis is a largely benign disease process that occurs secondary to infection with the Epstein-Barr virus. However, it can also present with more serious complications, including auto-immune hemolytic anemia and acute liver failure ...
Mark Forsberg, Mark Galan, Joshua Kra
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Rare Variants in PFIC‐Related Genes Among Adults With Intrahepatic Cholestasis
Hepatology Research, EarlyView.ABSTRACT Aim Biallelic pathogenic variants in progressive familial intrahepatic cholestasis (PFIC)‐related genes cause severe pediatric cholestasis. However, the clinical significance of heterozygous variants in adult intrahepatic cholestasis remains unclear.
Shunji Hirose +9 more
wiley +1 more source
Sangrias terapêuticas realizadas pelo Serviço de Hemoterapia do Hospital Universitário da Unversidade Federal de Santa Catarina (HU-UFSC). [PDF]
, 2008 Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina. Curso de Medicina.
Caixeta, Ananda Porto de Matos
core
Anemia with jaundice: An unusual cause
Medical Journal of Dr. D.Y. Patil University, 2015 Anemia and jaundice are two important clinical signs in medicine. Occurrence of these two signs together in a patient suggests hemolytic disorders. Hemochromatosis is a disease characterized by hyperpigmentation, arthralgia and diabetes.
K. V. S. Hari Kumar, A K Gupta
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Iron Overload: Pathophysiology, Diagnosis and Monitoring
International Journal of Laboratory Hematology, EarlyView.ABSTRACT Iron overload is associated with significant health risks, underscoring the importance of understanding its pathophysiology as well as establishing accurate diagnostic and monitoring methods. Chronic iron overload is associated with either genetic disorders characterized by excessive iron accumulation (hereditary hemochromatosis), or is ...
Elena Chatzikalil +3 more
wiley +1 more source
A Late Presentation of a Fatal Disease: Juvenile Hemochromatosis
Case Reports in Medicine, 2013 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.
Cynthia Cherfane +3 more
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