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分類 遺傳或先天性, 代謝, nephrology 頻率 少見 (U.S.) Usually seen in those 30 years or older.

然按年齡

然的症狀的持續時間

related physician types family practitioner internist nephrologist 郵政編碼 找到的地方 結果表明，電腦產生的建議，以幫助您找到一個醫生. MEDgle不推薦任何特定類型的醫生或聲稱是完整或準確的供應商和專業建議.

主要hyperoxaluria - 血壓升高引起腎結石草酸 定義 主要hyperoxaluria Primary hyperoxaluria is a rare condition characterized by the overproduction of a substance called oxalate (or oxalic acid). 更多 Primary hyperoxaluria is a rare condition characterized by the overproduction of a substance called oxalate (or oxalic acid). In the kidneys, the excess oxalate combines with calcium to form calcium oxalate, a hard compound that is the main component of kidney stones. Deposits of calcium oxalate can lead to kidney damage, kidney failure, and injury to other organs. less 一些常見的症狀 血壓高 尿痛女性 腳和腿腫 排尿少於正常 一些相關的診斷 1 - 7 of 40 診斷 糖尿病腎病 慢性腎小球腎炎 膜性腎小球腎炎 尿路梗阻 系統性紅斑狼瘡 hyperoxaluria 指甲髕骨綜合徵   更多 我有 '主要hyperoxaluria '? 此外，下列診斷測試可能需要幫助核實診斷: 診斷測試的搜索結果 '主要hyperoxaluria ' 1 - 5 of 26 診斷測試 24小時尿草酸 主要hyperoxaluria 和 24小時尿草酸 分子遺傳學研究 主要hyperoxaluria 和 分子遺傳學研究 饅頭 主要hyperoxaluria 和 饅頭 膳食問卷調查 主要hyperoxaluria 和 膳食問卷調查 KUB 主要hyperoxaluria 和 KUB Serum Creatinine 主要hyperoxaluria 和 Serum Creatinine 血清鈣 主要hyperoxaluria 和 血清鈣 超聲診斷腎臟輸尿管膀胱 主要hyperoxaluria 和 超聲診斷腎臟輸尿管膀胱 尿液分析 Examination of urine to detect disease 主要hyperoxaluria 和 尿液分析 螺旋CT尿路 主要hyperoxaluria 和 螺旋CT尿路 24小時尿鎂 the amount of magnesium that is excreted from the body 主要hyperoxaluria 和 24小時尿鎂 24小時尿鉀 the amount of potassium that is excreted from the body 主要hyperoxaluria 和 24小時尿鉀 24小時尿肌酐 主要hyperoxaluria 和 24小時尿肌酐 24小時尿液尿酸 主要hyperoxaluria 和 24小時尿液尿酸 24小時尿量 主要hyperoxaluria 和 24小時尿量 24-hour urine phosphate 主要hyperoxaluria 和 24-hour urine phosphate 尿枸櫞酸 主要hyperoxaluria 和 尿枸櫞酸 尿液pH值 主要hyperoxaluria 和 尿液pH值 24-hour urine calcium 主要hyperoxaluria 和 24-hour urine calcium 24-hour urine for oxalate 主要hyperoxaluria 和 24-hour urine for oxalate 24-hour urine sodium 主要hyperoxaluria 和 24-hour urine sodium 肝活檢 主要hyperoxaluria 和 肝活檢 飲食日記 主要hyperoxaluria 和 飲食日記 螺旋CT 主要hyperoxaluria 和 螺旋CT 尿電解質 主要hyperoxaluria 和 尿電解質 血清草酸 主要hyperoxaluria 和 血清草酸 欲了解更多請登錄，登錄是免費的（點擊登陸） 治療程序為 '主要hyperoxaluria '? 管理或治療疾病應始終取決於患者的衛生保健提供者. 以下是有關治療程序或藥物 primary hyperoxaluria: 治療程序的搜索結果 '主要hyperoxaluria ' 1 - 5 of 9 治療程序 rankings are computer generated. 請諮詢您的衛生保健提供者. 增加尿量 主要hyperoxaluria 和 增加尿量 肝，腎聯合移植 主要hyperoxaluria 和 肝，腎聯合移植 低草酸飲食 主要hyperoxaluria 和 低草酸飲食 減少肉類蛋白 主要hyperoxaluria 和 減少肉類蛋白 密集的透析治療 主要hyperoxaluria 和 密集的透析治療 透析治療 主要hyperoxaluria 和 透析治療 營養諮詢 主要hyperoxaluria 和 營養諮詢 飲食修改 主要hyperoxaluria 和 飲食修改 低脂肪飲食 主要hyperoxaluria 和 低脂肪飲食 欲了解更多請登錄，登錄是免費的（點擊登陸） 藥品的搜索結果 '主要hyperoxaluria ' 1 - 5 of 7 藥物 rankings are computer generated. 請諮詢您的衛生保健提供者.   pyridoxine 主要hyperoxaluria 和 pyridoxine   Potassium phosphate and sodium phophate 主要hyperoxaluria 和 Potassium phosphate and sodium phophate   hydrochlorothiazide 主要hyperoxaluria 和 hydrochlorothiazide   Oxalobacter formigenes 主要hyperoxaluria 和 Oxalobacter formigenes   Orthophosphate 主要hyperoxaluria 和 Orthophosphate   Magnesium oxide 主要hyperoxaluria 和 Magnesium oxide   pentosan polysulfate 主要hyperoxaluria 和 pentosan polysulfate 欲了解更多請登錄，登錄是免費的（點擊登陸） 網絡搜索結果 主要hyperoxaluria 網站（所有）  |  治療  |  藥品  |  測試  |  研究  |  飲食 結果 1 - 50 - 主要hyperoxaluria Primary hyperoxaluria - Wikipedia, the free encyclopedia [翻譯此頁] Primary hyperoxaluria results in increased excretion of oxalate, with oxalate ... Primary hyperoxaluria, on the other hand, refers to a specific type of ... http://en.wikipedia.org/wiki/Primary_hyperoxaluria   en.wikipedia.org - summary Primary hyperoxaluria - Genetics Home Reference [翻譯此頁] Primary hyperoxaluria is a rare condition characterized by the overproduction of ... Mutations in the AGXT and GRHPR genes cause primary hyperoxaluria. ... http://ghr.nlm.nih.gov/condition=primaryhyperoxaluria   ghr.nlm.nih.gov - summary Primary Hyperoxaluria Type 1 -- GeneReviews -- NCBI Bookshelf [翻譯此頁] In primary hyperoxaluria type 1, supersaturation of the urine with oxalate leads ... Primary hyperoxaluria was first described in the 1920s but not recognized as a ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=ph1   www.ncbi.nlm.nih.gov - summary Primary hyperoxaluria - OMIM - Genetic disorder catalog - Genetics Home ... [翻譯此頁] ... in the Genetics Home Reference condition summary on primary hyperoxaluria. OMIM topic: Hyperoxaluria, primary, type I. OMIM topic: Hyperoxaluria, primary, type II ... http://ghr.nlm.nih.gov/condition=primaryhyperoxaluria/show/OMIM   ghr.nlm.nih.gov - summary Primary Hyperoxaluria Type 2 -- GeneReviews -- NCBI Bookshelf [翻譯此頁] The age of onset of primary hyperoxaluria type 2 (PH2) is typically in childhood ... Primary hyperoxaluria type 1 (PH1) is caused by a deficiency of the liver ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=ph2   www.ncbi.nlm.nih.gov - summary Primary hyperoxaluria - Patient support - For patients and families ... [翻譯此頁] Genetic Conditions > primary hyperoxaluria > Patient support - For patients and ... in the Genetics Home Reference condition summary on primary hyperoxaluria. ... http://ghr.nlm.nih.gov/condition=primaryhyperoxaluria/show/Patient+support   ghr.nlm.nih.gov - summary Gene symbol: AGXT. Disease: primary hyperoxaluria type I. [翻譯此頁] 1: Hum Genet. 1999 May;104(5):441. Gene symbol: AGXT. Disease: primary hyperoxaluria type I. ... Hyperoxaluria, Primary/classification. Hyperoxaluria, Primary ... http://www.ncbi.nlm.nih.gov/pubmed/10394939   www.ncbi.nlm.nih.gov - summary Primary hyperoxaluria - References - Genetics Home Reference [翻譯此頁] Molecular aetiology of primary hyperoxaluria type 1. Nephron Exp Nephrol. ... D, Marangella M, Amoroso A. Primary hyperoxaluria: genotype-phenotype correlation. ... http://ghr.nlm.nih.gov/condition=primaryhyperoxaluria/show/References   ghr.nlm.nih.gov - summary Primary hyperoxaluria type 1 in Japan. [翻譯此頁] Primary hyperoxaluria type 1 in Japan. Ichiyama A, Oda T, Maeda-Nakai E. ... missing as in the case of primary hyperoxaluria type 1 (PH1) more glyoxylate is ... http://www.ncbi.nlm.nih.gov/pubmed/11330044?ordinalpos=2&ito...   www.ncbi.nlm.nih.gov - summary Primary hyperoxaluria - Related Gene(s) - Genetics Home Reference [翻譯此頁] Genetic Conditions > primary hyperoxaluria > Related Gene(s) ... Lister Hill National Center for Biomedical Communications ... Department of Health & Human ... http://ghr.nlm.nih.gov/condition=primaryhyperoxaluria/show/Related+Gene(s)   ghr.nlm.nih.gov - summary Primary hyperoxaluria type 2 in children. [翻譯此頁] Primary hyperoxaluria type 2 in children. Johnson SA, Rumsby G, Cregeen D, Hulton SA. ... The primary hyperoxalurias (PH1 and PH2) are rare defects of oxalate ... http://www.ncbi.nlm.nih.gov/pubmed/12185464   www.ncbi.nlm.nih.gov - summary Primary hyperoxaluria - Educational resources - Information pages ... [翻譯此頁] ... in the Genetics Home Reference condition summary on primary hyperoxaluria. Ask the Geneticist: Inheritance of Primary Hyperoxaluria. Madisons Foundation ... http://ghr.nlm.nih.gov/condition=primaryhyperoxaluria/show/Educational+resources   ghr.nlm.nih.gov - summary Primary hyperoxaluria. [翻譯此頁] ... Electrolyte Metab. 1994;20(6):340-51. Primary hyperoxaluria. Scheinman JI. ... Primary hyperoxaluria (PH) is a rare inborn error of amino acid metabolism, now ... http://www.ncbi.nlm.nih.gov/pubmed/7783696   www.ncbi.nlm.nih.gov - summary Primary hyperoxaluria - Gene Reviews - Clinical summary - Genetics Home ... [翻譯此頁] ... in the Genetics Home Reference condition summary on primary hyperoxaluria. Gene Review: Primary Hyperoxaluria, Type 1. Gene Review: Primary Hyperoxaluria, Type 2 ... http://ghr.nlm.nih.gov/condition=primaryhyperoxaluria/show/Gene+Reviews   ghr.nlm.nih.gov - summary Primary hyperoxaluria - MedlinePlus - Health information - Genetics ... [翻譯此頁] Genetic Conditions > primary hyperoxaluria > MedlinePlus - Health information ... in the Genetics Home Reference condition summary on primary hyperoxaluria. ... http://ghr.nlm.nih.gov/condition=primaryhyperoxaluria/show/MedlinePlus   ghr.nlm.nih.gov - summary Primary hyperoxaluria type 1 in Japan. [翻譯此頁] Primary hyperoxaluria type 1 in Japan. Takayama T, Nagata M, Ichiyama A, Ozono S. ... AIMS: Current status of primary hyperoxaluria (PH) has not been surveyed ... http://www.ncbi.nlm.nih.gov/pubmed/15961950?ordinalpos=1&ito...   www.ncbi.nlm.nih.gov - summary Molecular etiology of primary hyperoxaluria type 1: new directions for ... [翻譯此頁] Molecular etiology of primary hyperoxaluria type 1: new directions for treatment. ... Primary hyperoxaluria type 1 (PH1) is a rare autosomal-recessive disorder caused ... http://www.ncbi.nlm.nih.gov/pubmed/15961951   www.ncbi.nlm.nih.gov - summary Primary hyperoxaluria - Additional NIH Resources - National Institutes ... [翻譯此頁] ... primary hyperoxaluria > ... Home Reference condition summary on primary hyperoxaluria. ... National Institute of Diabetes and Digestive and Kidney ... http://ghr.nlm.nih.gov/condition=primaryhyperoxaluria/show/A...   ghr.nlm.nih.gov - summary Primary hyperoxaluria type 1: a cluster of new mutations in exon 7 of ... [翻譯此頁] Primary hyperoxaluria type 1: a cluster of new mutations in exon 7 of the ... Primary hyperoxaluria type 1 (PH1) is a severe autosomal recessive inborn error ... http://www.ncbi.nlm.nih.gov/pubmed/9192270   www.ncbi.nlm.nih.gov - summary Primary hyperoxaluria [翻譯此頁] Primary hyperoxaluria type 1is a rare metabolic disorder transmitted as an ... Primary hyperoxaluria, calcium-oxalate deposition, Glyoxalate, L-alanine: ... http://www.orpha.net/data/patho/GB/uk-oxalos.pdf   www.orpha.net - summary Hyperoxaluria, Primary (Type I) - Yahoo! Health [翻譯此頁] Important It is possible that the main title of the report Hyperoxaluria, Primary (Type I) is not the name you expected. Please check the synonyms listing to find ... http://health.yahoo.com/urinary-overview/hyperoxaluria-prima...   health.yahoo.com - summary Primary hyperoxaluria type I due to a point mutation of T to C in the ... [翻譯此頁] Primary hyperoxaluria type I due to a point mutation of T to C in the coding ... constructed from the liver of a primary hyperoxaluria type I (PH1) case in which ... http://www.ncbi.nlm.nih.gov/pubmed/2039493   www.ncbi.nlm.nih.gov - summary Primary hyperoxaluria type 1 and peroxisome-to-mitochondrion ... [翻譯此頁] Primary hyperoxaluria type 1 and peroxisome-to-mitochondrion mistargeting of ... with the autosomal recessive disease primary hyperoxaluria type 1, there is a ... http://www.ncbi.nlm.nih.gov/pubmed/8507692   www.ncbi.nlm.nih.gov - summary Liver transplantation for type 1 primary hyperoxaluria as a cure for ... [翻譯此頁] Liver transplantation for type 1 primary hyperoxaluria as a cure for combined thrombophilia. ... Hyperoxaluria, Primary/surgery* Kidney Transplantation. Liver ... http://www.ncbi.nlm.nih.gov/pubmed/15543348?ordinalpos=15&it...   www.ncbi.nlm.nih.gov - summary Oxalosis and Hyperoxaluria [翻譯此頁] This information is provided as a resource and does not constitute an ... professionals in the field of primary hyperoxaluria and oxalate stone disease. ... http://www.webmd.com/a-to-z-guides/oxalosis-and-hyperoxaluria   www.webmd.com - summary Talk:Primary hyperoxaluria - Wikipedia, the free encyclopedia [翻譯此頁] Talk:Primary hyperoxaluria. From Wikipedia, the free encyclopedia. Jump to: navigation, search. This article is within the scope of WikiProject Medicine. ... http://en.wikipedia.org/wiki/Talk:Primary_hyperoxaluria   en.wikipedia.org - summary Kidney Stones [翻譯此頁] Hyperoxaluria is defined as either primary or secondary. Primary hyperoxaluria is an inherited disorder in which excess oxalate in the ... http://adam.about.com/reports/000081_2.htm   adam.about.com - summary Oxalosis - NextBio [翻譯此頁] Oxalosis in primary hyperoxaluria in infancy : Report of a case in a 3-month-old ... Primary hyperoxaluria (PH1) is a rare inborn autosomal recessive metabolic ... http://www.nextbio.com/b/home/home.nb?q=oxalosis   www.nextbio.com - summary Tubulointerstitial Nephritis: Tubulointerstitial Diseases: Merck Manual ... [翻譯此頁] Tubulointerstitial nephritis can be primary or can be secondary to glomerular ... (types I and II primary hyperoxaluria) or acquired GI diseases (eg, short bowel ... http://www.merck.com/mmpe/sec17/ch236/ch236c.html   www.merck.com - summary Oxalosis and Hyperoxaluria - Yahoo! Health [翻譯此頁] ... professionals in the field of primary hyperoxaluria and oxalate stone disease. ... Oxalosis and Hyperoxaluria Fdn. 201 East 19th Street, #12E. New York, NY 10003 ... http://health.yahoo.com/urinary-resources/oxalosis-and-hyper...   health.yahoo.com - summary Kidney stones [翻譯此頁] Hyperoxaluria can be either primary or secondary. Primary hyperoxaluria is an inherited disorder in which too much oxalate in the ... http://adam.about.com/reports/Kidney-stones.htm   adam.about.com - summary New York Methodist Hospital [翻譯此頁] Hyperoxaluria can be either primary or secondary. Primary hyperoxaluria is an inherited disorder in which too much oxalate in the ... http://nymethodist.adam.com/content.aspx?productId=10&pid=10&gid=000081   nymethodist.adam.com - summary Primary hyperoxaluria - Gene Tests - DNA tests ordered by healthcare ... [翻譯此頁] Genetic Conditions > primary hyperoxaluria > ... on primary hyperoxaluria. Gene Tests: Hyperoxaluria, Primary, Type 1. Gene Tests: Hyperoxaluria, Primary, Type ... http://ghr.nlm.nih.gov/condition=primaryhyperoxaluria/show/Gene+Tests   ghr.nlm.nih.gov - summary AGXT - alanine-glyoxylate aminotransferase - Genetics Home Reference [翻譯此頁] primary hyperoxaluria - caused by mutations in the AGXT gene ... As a result, glyoxylate accumulates, leading to the signs and symptoms of primary hyperoxaluria. ... http://ghr.nlm.nih.gov/gene=agxt   ghr.nlm.nih.gov - summary A United States survey on diagnosis, treatment, and outcome of primary ... [翻譯此頁] A United States survey on diagnosis, treatment, and outcome of primary hyperoxaluria. ... Primary hyperoxaluria (PH) is a heterogeneous disease with a variable age of ... http://www.ncbi.nlm.nih.gov/pubmed/12920626   www.ncbi.nlm.nih.gov - summary AGXT - References - Genetics Home Reference [翻譯此頁] Preliminary Evidence for Ethnic Differences in Primary Hyperoxaluria Type 1 Genotype. ... Molecular aetiology of primary hyperoxaluria type 1. Nephron Exp Nephrol. ... http://ghr.nlm.nih.gov/gene=agxt/show/References   ghr.nlm.nih.gov - summary Mistargeting of peroxisomal L-alanine:glyoxylate aminotransferase to ... [翻譯此頁] In approximately one-third of primary hyperoxaluria type 1 patients, disease is ... with reference to the AGT targeting defect in primary hyperoxaluria and also ... http://www.ncbi.nlm.nih.gov/pubmed/1961759   www.ncbi.nlm.nih.gov - summary The gene encoding hydroxypyruvate reductase (GRHPR) is mutated in ... [翻譯此頁] ... reductase (GRHPR) is mutated in patients with primary hyperoxaluria type II. ... Primary hyperoxaluria type II (PH2) is a rare monogenic disorder that is ... http://www.ncbi.nlm.nih.gov/pubmed/10484776   www.ncbi.nlm.nih.gov - summary Food, nutrition, and metabolism - Genetics Home Reference [翻譯此頁] D-glycerate dehydrogenase deficiency see primary hyperoxaluria ... glyceric aciduria see primary hyperoxaluria. glycine encephalopathy ... http://ghr.nlm.nih.gov/conditionCategory=foodnutritionandmetabolism   ghr.nlm.nih.gov - summary Diagnostic and therapeutic approaches in patients with secondary ... [翻譯此頁] Secondary hyperoxaluria is due either to increased intestinal oxalate absorption ... urinary oxalate excretion is usually lower than in primary hyperoxaluria, it may ... http://www.ncbi.nlm.nih.gov/pubmed/12957811   www.ncbi.nlm.nih.gov - summary Hyperoxaluria - Wikipedia, the free encyclopedia [翻譯此頁] A child with primary hyperoxaluria was treated with a liver and kidney transplant.[2] ... "Primary hyperoxaluria - Genetics Home Reference" ... http://en.wikipedia.org/wiki/Hyperoxaluria   en.wikipedia.org - summary GRHPR - glyoxylate reductase/hydroxypyruvate reductase - Genetics Home ... [翻譯此頁] primary hyperoxaluria - caused by mutations in the GRHPR gene ... more than a dozen GRHPR mutations that cause type 2 primary hyperoxaluria. ... http://ghr.nlm.nih.gov/gene=grhpr   ghr.nlm.nih.gov - summary Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary ... [翻譯此頁] Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type I. ... that primary hyperoxaluria type I should be added to the rather ... http://www.ncbi.nlm.nih.gov/pubmed/3709805   www.ncbi.nlm.nih.gov - summary GRHPR - References - Genetics Home Reference [翻譯此頁] ... metabolism: implications for primary hyperoxaluria. Am J Nephrol. ... Pirulli D, Marangella M, Amoroso A. Primary hyperoxaluria: genotype-phenotype correlation. ... http://ghr.nlm.nih.gov/gene=grhpr/show/References   ghr.nlm.nih.gov - summary Enzymological and mutational analysis of a complex primary ... [翻譯此頁] ... analysis of a complex primary hyperoxaluria type 1 phenotype involving ... Primary hyperoxaluria type 1 (PH1) is a rare autosomal recessive disease caused ... http://www.ncbi.nlm.nih.gov/pubmed/8101040   www.ncbi.nlm.nih.gov - summary Should liver transplantation be performed before advanced renal ... [翻譯此頁] Primary hyperoxaluria type 1 (PH1) is a rare recessive autosomal inborn error of ... Hyperoxaluria, Primary/complications* Kidney Failure, Chronic/diagnosis ... http://www.ncbi.nlm.nih.gov/pubmed/8476723   www.ncbi.nlm.nih.gov - summary Genomics|HuGENet|Literature|2007 May 3 [翻譯此頁] The mission of the National Office of Public Health Genomics is to integrate advances in human genetics into ... 1 Primary Hyperoxaluria Shows Feasibility ... http://www.cdc.gov/genomics/hugenet/literature/2007/Hmay03.htm   www.cdc.gov - summary Kidneys and urinary system - Genetics Home Reference [翻譯此頁] D-glycerate dehydrogenase deficiency see primary hyperoxaluria ... primary hyperoxaluria. Primary hyperuricemia syndrome see Lesch-Nyhan syndrome ... http://ghr.nlm.nih.gov/conditionCategory=kidneysandurinarysystem   ghr.nlm.nih.gov - summary Identification of missense, nonsense, and deletion mutations in the ... [翻譯此頁] ... mutations in the GRHPR gene in patients with primary hyperoxaluria type II (PH2) ... Primary hyperoxaluria type II (PH2) is a rare disease characterized by the ... http://www.ncbi.nlm.nih.gov/pubmed/11030416   www.ncbi.nlm.nih.gov - summary A glycine-to-glutamate substitution abolishes alanine:glyoxylate ... [翻譯此頁] ... catalytic activity in a subset of patients with primary hyperoxaluria type 1. ... primary hyperoxaluria type 1 (PH1) patient who had normal levels of hepatic ... http://www.ncbi.nlm.nih.gov/pubmed/1349575   www.ncbi.nlm.nih.gov - summary 查看更多 1  2