MALADIE DE CACCHI RICCI PDF

Archives de pédiatrie – Vol. 11 – N° 1 – p. – La maladie de Cacchi et Ricci chez un enfant de 13 ans – EM|consulte. Kidney Int. Feb;69(4) Medullary sponge kidney (Lenarduzzi-Cacchi -Ricci disease): a Padua Medical School discovery in the s. Gambaro G(1). Cette page est une page de collecte et de diffusion d’informations concernant la maladie de cacchi-ricci (Medullary Sponge Kidney). Venez partager vos.

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A rare, autosomal recessive form malaxie associated with Caroli disease. Cacchi-Ricci syndrome Related people Roberto Cacchi Vincenzo Ricci A congenital cystic disease of the pyramids with dilation of the terminal collecting ducts in the kidneys and multiple small cysts in the medulla, giving the kidneys a spongy appearance.

Cacchi-Ricci syndrome

American Journal of Roentgenology. Other search option s Alphabetical list. Views Read Edit View history. Onset of detection from 3 weeks of age to 71 years, both sexes equally affected.

The irregular ectatic collecting ducts are often seen in MSK, which are sometimes described as having a “paintbrush-like” appearance, are best seen on intravenous urography.

Archived from the original PDF on Retrieved 21 May Narcotic medication even with large quantities is sometimes not adequate. La maladie de Cacchi et Ricci chez un enfant de 13 ans.

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Medullary sponge kidney – Wikipedia

An eponym is a word derived from the name of a person, whether real or fictional. Uncomplicated form usually asymptomatic. However, other data related to the disease are accessible from the Additional Information menu located at the bottom of this page. Congenital malformations and deformations of urinary system Q60—Q64 The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.

As per the Law relating to information storage and personal integrity, you have the right to oppose art 26 of that lawaccess art 34 of that law and rectify art 36 of that law your personal data.

It is our ambition to present a complete survey of all amladie phenomena named for a person, with a biography of that person. Non-obstructing stones in MSK can be associated with significant and chronic pain even if they’re not passing.

If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned here: A medical eponym is thus any word related to medicine, whose name is derived from a person.

While some patients report increased chronic kidney pain, the source of the pain, when a UTI or blockage is not present, is unclear at this time.

You can move this window by clicking on the headline. Infobox medical condition new. Access to the full text of this article requires a subscription. Personal caccui regarding our website’s visitors, including their identity, is confidential. If you want to subscribe to this journal, see our rates You can purchase this item in Pay Per View: Specialised Social Services Eurordis directory.

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The pain in this situation can be constant. Retrieved 1 January From Wikipedia, fe free encyclopedia. Harrison’s Principles of Internal Medicine 18th ed.

MSK was previously believed not to be hereditary but there is more evidence coming forth that may indicate otherwise. Health care resources for this disease Expert centres Diagnostic tests 1 Patient organisations 13 Orphan ,aladie s 0. This survey of medical eponyms and the persons behind them is meant as a general interest site only. In addition to the amladie clinical phenotype of recurrent stone disease, other clinical profiles have now been recognized, that is, an indolent, almost asymptomatic MSK, and a rare form characterized by intractable pain.

In the general population, the frequency of medullary sponge kidney disease is reported to be 0.