A collection of disease information resources and questions answered by our Genetic and Rare Diseases Information Specialists for Medullary sponge kidney. NOTICE Undefined index: PDF (includes_ws_v2/controladores/). HIPOKALIEMIA SINTOMÁTICA ASOCIADA A ENFERMEDAD DE CACCHI – RICCI. V. Esteve, N. Fontseré, A. Saurina, X. Cuevas. Read. Times was read.
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Poster actions add bookmark contact presenter send a friend download pdf. All content on this website, including dictionary, thesaurus, literature, geography, and other reference data is for informational purposes only. Medullary sponge kidney is associated with several developmental and genetic disorders including the following conditions. The Journal publishes articles on basic or clinical research relating to nephrology, arterial hypertension, dialysis and kidney transplants.
In a normal kidney, urine flows through these tubules as it is being formed. The journal accepts submissions of articles in English and in Spanish languages. Only comments written in English can be processed. You can change the settings or obtain more information by clicking here.
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Also known as lenarduzzi cacchiricci disease, medullary sponge kidney is a congenital developmental abnormality characterized by ectasia and cystic dilatation of the intrapyramidal or caccho-ricci portions of the renal medullary collecting ducts. Are you a health professional able to prescribe or dispense drugs? You can change the settings or obtain more cacchi-rucci by clicking here.
The documents contained in this web site are presented for cacchi-icci purposes only. SRJ is a prestige metric based on the idea that not all citations are the same.
HIPOKALIEMIA SINTOMÁTICA ASOCIADA A ENFERMEDAD DE CACCHI-RICCI
An Orphanet summary for this disease is currently under development. Medullary sponge kidney also known as cacchiricci disease is a congenital disorder of the kidneys characterized by cystic dilatation of the collecting tubules in one or both kidneys. SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field.
Medullary cystic kidney is a rare inherited kidney disease nephropathy characterized by excessive amounts of urea and other waste products in the urine uremia. In msk, tiny sacs called cysts form in the medulla the inner part of the kidney, creating a spongelike appearance. Home Articles in press Archive. Si continua navegando, consideramos que acepta su uso. The journal accepts submissions of articles in English and in Spanish languages. Medullary sponge kidney nord national organization for.
SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field. Summary An Orphanet summary for this disease is currently under development. This work is licensed under a Creative Commons Attribution 4.
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Pdf symptomatic hypokalemia associated with cacchiricci. Cacchi ricci disease, precalyceal canalicular ectasia, cacchiricci syndrome, sponge kidney, cystic dilatation of renal collecting tubes megalocytic interstitial nephritis synonyms.
Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted.
Bibliografia y lecturas recomendadas ascitis urinosa en. CiteScore measures average citations received per document published. Medullary sponge kidney is usually cacchi-rlcci benign condition, and patients can remain asymptomatic.
National kidney foundation genetic and rare diseases. Health care resources for this disease Expert centres Diagnostic tests 1 Patient organisations 13 Orphan drug s 0. Other search option s Alphabetical list.
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Enfermedad de cacchi-ricci pdf
Medullary sponge kidney msk is a birth defect of the tubules tiny tubes inside the kidneys. The Impact Factor measures the average number of citations received in a particular year by papers published in the journal during the two enermedad years. For all other comments, please send your remarks via contact us. The file contains 5 pages and is free to view, download or print.
To improve our services and products, we use “cookies” own or third parties authorized to show advertising related to client preferences through the analyses of navigation customer behavior. Additional information Further information on this disease Classification enfemedad 3 Gene s 0 Clinical signs and symptoms Other website s 3.
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