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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Personal information regarding our website’s visitors, including their identity, is confidential. Summary An Orphanet summary for this disease is currently under development. Mxladie Urachal cyst Urachal fistula Urachal sinus. Journal page Archives Contents list. Current Opinion in Nephrology and Hypertension.

In addition to riccii 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. By using this site, you agree to the Terms of Use and Privacy Policy.

American Journal of Roentgenology. La maladie de Cacchi et Ricci chez un enfant de 13 ans. Retrieved 22 August As per the Law relating to information storage cacchl 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.

Views Read Edit View history. 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. Access to the full text of this article requires a subscription.


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. Additional information Further information on this disease Classification s 3 Gene s 0 Clinical signs and symptoms Other website s 3.

Cacchi-Ricci syndrome

Families with autosomal dominant inheritance reported. Curr Opin Nephrol Hypertens. A rare, autosomal recessive form is associated with Caroli rivci. Classically, MSK is seen as hyperechoic papillae with clusters of small stones on ultrasound examination of the kidney or with an abdominal x-ray. The owners of this website hereby guarantee to respect the legal confidentiality conditions, applicable in France, and not to disclose this data to third parties.

Check malaide box if you wish to receive a copy of your message. Onset of detection from 3 weeks of age to 71 years, both sexes equally affected.

Narcotic medication even with large quantities is sometimes not adequate. Retrieved from ” https: This page was last edited on 2 Octoberat Specialised Social Services Eurordis directory. Access to the PDF text. maladoe

Cacchi-Ricci syndrome

Ectopic ureter Megaureter Duplicated ureter. From Wikipedia, the free encyclopedia. An Orphanet summary for this disease is currently under development. Access to the malade HTML. D ICD – Patients with the more rare form of MSK marked by chronic pain typically require pain management. Often, aggressive treatment is unnecessary for people with MSK disease that does not cause any symptoms asymptomatic.

Urachal cyst Caxchi fistula Urachal sinus. Epispadias Hypospadias Posterior urethral valves. Uncomplicated form usually asymptomatic. 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. This pain can often be mmaladie and treatment is challenging.


Medullary sponge kidney – Wikipedia

In patients with low levels of citrate in the urine hypocitraturia and incomplete distal renal tubular acidosistreatment with cacchi citrate helps prevent the formation of new kidney stones. It is our ambition to present a complete survey of all medical phenomena named for a person, with a biography of that person.

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Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. In the general population, the frequency ,aladie medullary sponge kidney disease is reported to be 0. Congenital disorders of urinary system Kidney diseases. What is an eponym? Individuals with medullary sponge kidney are at increased risk for kidney stones and urinary tract infection UTI. Frequently congenital and familial. A medical eponym is thus any word related to medicine, whose name is derived from a person.