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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In addition to the typical 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.

Maladie de Cacchi-Ricci

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Atti della Societa Italiana di Urologia, Current Opinion in Nephrology and Hypertension. An Orphanet summary for this disease is currently under development. A rare, autosomal recessive form is associated with Caroli disease.

Retrieved 22 August This explains why so many tubular defects coexist in this disease, and particularly a distal tubular acidification defect of which the highly prevalent metabolic bone disease is one very important consequence.

Medullary sponge kidney also known as Cacchi—Ricci disease is a congenital disorder of the kidneys characterized by cystic dilatation of the collecting tubules in one or both kidneys.

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In the general population, the frequency of medullary sponge kidney disease is reported to be 0. American Journal of Roentgenology. For all other comments, please send your remarks via contact us. Only comments written in English can be processed. However, IV urography has been largely replaced by contrast-enhanced, high-resolution helical CT with digital reconstruction. Congenital malformations and deformations of urinary system Q60—Q64 ve, Check this box if you wish to receive a copy of your message.

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. Outline Masquer le plan.

No information found here must under any circumstances be used for medical purposes, diagnostically, therapeutically or otherwise. Retrieved 21 May Summary and related texts.

Families with autosomal dominant inheritance reported. Often, aggressive treatment is unnecessary for people with MSK disease that does not cause any symptoms asymptomatic. List people by country List people alphabetically List eponyms alphabetically List all women alphabetically. D ICD – The documents contained in this web site are presented for information purposes only.

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Curr Opin Nephrol Hypertens. While some patients report increased chronic kidney caccui, the source of the pain, when a UTI or blockage is not present, is unclear at this time. This survey of medical eponyms and the persons behind them is meant as a general interest site only.

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Urachal cyst Urachal fistula Urachal sinus.

Infobox medical condition new. Frequently congenital and familial. Hematuria ; Kidney sponge ; Kidney diseases ; Lithiasis ; Child. You can move this window by clicking on the headline. If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned here: Other search option s Alphabetical list. Health care resources for this disease Expert centres Diagnostic tests 1 Patient organisations 13 Orphan drug s 0.

An eponym is a word derived from the name of a person, whether real or fictional.

Orphanet: Maladie de Cacchi Ricci

Ectopic ureter Megaureter Duplicated ureter. Medullary sponge as seen on an intravenous pyelogram. Medical geneticsNephrology. Views Read Edit View history. This pain can often be debilitating and treatment is challenging. The pain in this situation can be constant. Patients with the more rare form of MSK marked by chronic pain typically require pain management.

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La maladie de Cacchi et Ricci chez un enfant de 13 ans – EM|consulte

Top of the page – Article Outline. The irregular ectatic collecting ducts are often seen in MSK, which jaladie sometimes described as having a “paintbrush-like” appearance, are best seen on intravenous urography.

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