Αποτελέσματα Αναζήτησης
6 Οκτ 2024 · The condition is typically diagnosed in middle age; women are often diagnosed later in life due to the iron loss associated with menstruation. Symptoms are generally nonspecific, and many cases are discovered through elevated transaminase, ferritin, and transferrin saturation levels.
17 Ιουλ 2023 · Apply best practices when utilizing laboratory and other diagnostic testing to monitor disease progression in patients with hereditary hemochromatosis. Develop and implement interprofessional team processes to improve outcomes and prevent complications in patients with hereditary hemochromatosis.
19 Μαΐ 2022 · Here we present recommendations for unambiguous HC classification developed by a working group of the International Society for the Study of Iron in Biology and Medicine (BIOIRON Society), including both clinicians and basic scientists during a meeting in Heidelberg, Germany.
There is often an associated chondrocalcinosis. Why: hemochromatosis is an autosomal recessive disease that produces an arthritis similar to osteoarthritis or pseudogout. How: hemochromatosis is diagnosed by the typical physical and radiographic findings supported by elevated serum iron concentrations and high transferrin saturations.
5 Απρ 2018 · Diagnosis is noninvasive and includes clinical examination, assessment of plasma iron parameters, imaging and genetic testing. The mainstay therapy is phlebotomy, although iron chelation can be used in some patients.
Untreated hemochromatosis can lead to chronic liver disease, fibrosis, cirrhosis, and hepatocellular carcinoma (HCC). Many invasive and noninvasive diagnostic tests are available to aid in diagnosis and treatment.
9 Σεπ 2022 · HH was first defined in 2011 ICD-9 as a separate diagnosis in the NIS dataset; the HH cohort is extracted from January 2011 to December 2019 using 275.01 (ICD-9) and E83.110 (ICD-10) diagnosis codes of HH.
