MALADIE DE CACCHI RICCI PDF

Only comments written in English can be processed. La maladie de Cacchi et Ricci chez un enfant de 13 ans — EM consulte 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. Access to the text HTML. 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. Classically, MSK is seen as hyperechoic papillae with clusters of small stones on ultrasound examination of the kidney or with an abdominal x-ray. Access to the PDF text.

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Faezilkree Summary An Orphanet summary for this disease is currently under development. Other search option s Alphabetical list. American Journal of Roentgenology. This page was last mqladie on 2 Octoberat The material is in no way intended to replace professional medical care by a riccci specialist and should not be used as a basis for diagnosis or treatment. Curr Opin Nephrol Hypertens. 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.

Access to the text HTML. Access to the full text of this article requires a caccgi. 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 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.

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By using this site, you malafie to the Terms of Use and Privacy Policy. However, IV urography has been largely replaced by contrast-enhanced, high-resolution helical CT with digital reconstruction. 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.

Ectopic ureter Megaureter Duplicated ureter. There was a problem providing the content you requested A rare, autosomal recessive form is associated with Caroli disease. 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.

Most cases are asymptomatic or are discovered during an investigation of blood in the urine. Current Opinion in Nephrology and Hypertension. 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, excruciating pain.

Additional information Further information on this disease Classification s 3 Gene s 0 Clinical signs and symptoms Other website s 3. It is not certain what causes this pain but researchers have proposed that the small numerous stones seen in MSK may cause obstruction of the small tubules and collecting ducts in the kidney which could lead to the pain.

Narcotic medication even with large quantities is sometimes not adequate. Congenital disorders of urinary system Kidney diseases. In patients with low levels of citrate in the urine hypocitraturia and incomplete distal renal tubular acidosistreatment with potassium citrate helps prevent the formation of new kidney stones.

La maladie de Cacchi et Ricci chez un enfant de 13 ans — EM consulte If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned here: From Wikipedia, the free encyclopedia. Medical geneticsNephrology. What is an eponym? For all other comments, please send your remarks via contact us.

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. Epispadias Hypospadias Posterior urethral valves.

Urachal cyst Urachal fistula Urachal sinus. Atti della Societa Italiana di Urologia, However, other data related to maadie disease are accessible from the Additional Information menu located at the bottom of this page. List people by country List people alphabetically List eponyms alphabetically List all women alphabetically. Outline Masquer le plan. An eponym is a word derived from the name of a person, whether real or fictional. Only comments written in English can be processed. The documents contained in this web site are presented for information purposes only.

La maladie de Cacchi et Ricci chez un enfant de 13 ans. You can move this window by clicking on the headline. Check this box if you wish to receive a copy of your message. Maladie de Cacchi-Ricci Medullary sponge as seen on an intravenous pyelogram. This survey of medical eponyms and the persons behind them is meant as a general interest site only.

It is our ambition to present a complete survey of all medical phenomena named for a person, with a biography of that person. D ICD — Classically, MSK is seen maadie hyperechoic papillae with naladie of small stones on ultrasound examination of the kidney or with an abdominal x-ray. Related Articles.

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