Universitari general vall dhebron barcelona barcelona en colaboracion con. For language access assistance, contact the ncats public information officer. If you have problems viewing pdf files, download the latest version of adobe reader. Neurological manifestations in erdheimchester disease. Ecd causes the overproduction of immune cells called histiocytes, which then accumulate in tissues and organs in the body. It was declared a histiocytic neoplasm by the world health organization in 2016. Langerhans cell histiocytosis and erdheimchester disease. Pdf erdheimchester disease is a rare systemic xanthogranulomatous disease of unknown aetiology in which there is an abnormal.
A read is counted each time someone views a publication summary such as the title, abstract, and list of authors, clicks on a figure, or views or downloads the fulltext. Parts of the body that may be involved include the long bones, retroperitoneum, skin, eyes and eyelids, lungs. Pdf we report a 76yearold male who was admitted due to progressive congestive heart failure lasting several months. All structured data from the file and property namespaces is available under the creative commons cc0 license. Erdheimchester disease ecd is a rare condition that can affect many parts of the body. Genetic and rare diseases information center gard po box 8126, gaithersburg, md 208988126 tollfree. Erdheim chester disease ecd is a rare condition that can affect many parts of the body.
It has been diagnosed in children, but it most commonly affects adults. Erdheimchester disease ecd is a nonlangerhans cell form of. Files are available under licenses specified on their description page. Erdheimchester disease genetic and rare diseases information.
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