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Erdheim-Chester disease is associated with high mortality rates.
House first suspects it is Erdheim-Chester disease and orders a colonoscopy, but tests are negative.
House then orders his team to perform the final test on the first disease suggested: Erdheim-Chester disease.
Proptosis can also be a sign of an ultra-rare disorder called Erdheim-Chester Disease.
Erdheim-Chester disease.
He is credited with the characterization (or partial characterization) of Erdheim-Chester disease and cystic medial necrosis.
Additional information about Erdheim-Chester Disease can be obtained from the ECD Global Alliance.
Others in this category are Erdheim-Chester disease (primarily found in adults) and juvenile xanthogranuloma (diagnosed in children and adults).
The Erdheim-Chester Disease Global Alliance is a support and advocacy group with the goal of raising awareness of and promoting research into ECD.
ECD Lipoid Granulomatosis None Erdheim-Chester disease (ECD) is a rare multisystem disorder of adulthood.
Examples of such lesions are: pleural plaques, thoracic splenosis, catamenial pneumothorax, pleural pseudotumor, diffuse pleural thickening, diffuse pulmonary lymphangiomatosis and Erdheim-Chester Disease.
In view of the familial nature of these findings, members of this dynasty likely suffered from a multi-organ fibrotic condition such as Erdheim-Chester disease or a familial multifocal fibrosclerosis where thyroiditis, obesity and ocular proptosis may have all occurred concurrently.
Erdheim-Chester disease (also known as Erdheim-Chester syndrome or polyostotic sclerosing histiocytosis) is a rare disease characterized by the abnormal multiplication of a specific type of white blood cells called histiocytes, or tissue macrophages (technically, this disease is termed a non-Langerhans-cell histiocytosis).
Erdheim-Chester disease (also known as Erdheim-Chester syndrome or polyostotic sclerosing histiocytosis) is a rare disease characterized by the abnormal multiplication of a specific type of white blood cells called histiocytes, or tissue macrophages (technically, this disease is termed a non-Langerhans-cell histiocytosis).
Erdheim-Chester disease (also known as Erdheim-Chester syndrome or polyostotic sclerosing histiocytosis) is a rare disease characterized by the abnormal multiplication of a specific type of white blood cells called histiocytes, or tissue macrophages (technically, this disease is termed a non-Langerhans-cell histiocytosis).