から減少の結果

780 B

124 M

16 M

418

359

to ~80 options

options split into images, definition, symptoms, related diagnoses, diagnostic tests, therapies, and medications

カテゴリ 先天性遺伝子オレゴン, 代謝, 腎臓病 周波数 珍しい (U.S.) Usually seen in those 30 years or older.

年齢によって起こりやすくなります

症状のある期間で可能

関連医師の種類 family practitioner internist nephrologist 郵便番号 して下さいローカル その結果、コンピュータを見つけるのに役立つ場合は医師のアドバイスに生成される. MEDgleを完了させるかは、プロバイダとの専門医師やクレームの正確な提案では特定のタイプをお勧めしていません.

原発性シュウ酸尿 - 増加血液が腎臓結石を引き起こしてシュウ酸 に定義されています 原発性シュウ酸尿 Primary hyperoxaluria is a rare condition characterized by the overproduction of a substance called oxalate (or oxalic acid). よりたくさんの 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 いくつかの共通の現象 高血圧 女性の痛みを伴う排尿 腫れ足と脚 以下、通常よりも排尿 いくつかの関連診断 1 - 7 of 79 診断 急性腎不全 急性尿細管壊死 尿路閉塞 ループス腎炎 シスチン尿 腎動脈閉塞 膜性糸球体腎炎   より 私はありますか？ '原発性シュウ酸尿'? 加えて、以下の診断テストをされるとの診断に役立つかどうかを確認する必要があります: 診断テストの検索結果を得るために '原発性シュウ酸尿' 1 - 5 of 26 診断テスト 24時間尿中シュウ酸 原発性シュウ酸尿 および 24時間尿中シュウ酸 分子遺伝学的研究 原発性シュウ酸尿 および 分子遺伝学的研究 尿素 原発性シュウ酸尿 および 尿素 食生活アンケート 原発性シュウ酸尿 および 食生活アンケート KUB 原発性シュウ酸尿 および KUB 血清クレアチニン 原発性シュウ酸尿 および 血清クレアチニン 血清カルシウム 原発性シュウ酸尿 および 血清カルシウム 超音波検査は、尿管膀胱腎臓 原発性シュウ酸尿 および 超音波検査は、尿管膀胱腎臓 尿検査 Examination of urine to detect disease 原発性シュウ酸尿 および 尿検査 らせんCT尿路 原発性シュウ酸尿 および らせんCT尿路 24時間尿マグネシウム the amount of magnesium that is excreted from the body 原発性シュウ酸尿 および 24時間尿マグネシウム 24時間尿中カリウム the amount of potassium that is excreted from the body 原発性シュウ酸尿 および 24時間尿中カリウム 24時間尿クレアチニン 原発性シュウ酸尿 および 24時間尿クレアチニン 24時間尿中尿酸 原発性シュウ酸尿 および 24時間尿中尿酸 24時間尿量 原発性シュウ酸尿 および 24時間尿量 24時間尿酸 原発性シュウ酸尿 および 24時間尿酸 尿酸 原発性シュウ酸尿 および 尿酸 尿のpH 原発性シュウ酸尿 および 尿のpH 24-hour urine calcium 原発性シュウ酸尿 および 24-hour urine calcium 24-hour urine for oxalate 原発性シュウ酸尿 および 24-hour urine for oxalate 24-hour urine sodium 原発性シュウ酸尿 および 24-hour urine sodium 生検肝 原発性シュウ酸尿 および 生検肝 ダイエット日記 原発性シュウ酸尿 および ダイエット日記 スパイラルCT検査 原発性シュウ酸尿 および スパイラルCT検査 尿中電解質 原発性シュウ酸尿 および 尿中電解質 血清シュウ 原発性シュウ酸尿 および 血清シュウ 詳細については、ログインしてください、ログイン情報（クリックしてログインする）無料です 治療の手順を '原発性シュウ酸尿'? 常に患者さんの健康管理や介護のプロバイダによって決定されるべき疾患の治療. 下記の手順または関連する治療薬の一覧です primary hyperoxaluria: 治療の手順の検索結果 '原発性シュウ酸尿' 1 - 5 of 9 治療の手順 ランキングは、コンピュータが生成されます. あなたの健康管理プロバイダを参照してください. 増加尿量 原発性シュウ酸尿 および 増加尿量 肝腎移植 原発性シュウ酸尿 および 肝腎移植 低シュウ酸ダイエット 原発性シュウ酸尿 および 低シュウ酸ダイエット 縮小肉タンパク質 原発性シュウ酸尿 および 縮小肉タンパク質 集中透析 原発性シュウ酸尿 および 集中透析 透析 原発性シュウ酸尿 および 透析 栄養カウンセリング 原発性シュウ酸尿 および 栄養カウンセリング 食事の変更 原発性シュウ酸尿 および 食事の変更 低脂肪の食事をする 原発性シュウ酸尿 および 低脂肪の食事をする 詳細については、ログインしてください、ログイン情報（クリックしてログインする）無料です 薬の検索結果 '原発性シュウ酸尿' 1 - 5 of 7 薬 ランキングは、コンピュータが生成されます. あなたの健康管理プロバイダを参照してください.   pyridoxine 原発性シュウ酸尿 および pyridoxine   Potassium phosphate and sodium phophate 原発性シュウ酸尿 および Potassium phosphate and sodium phophate   hydrochlorothiazide 原発性シュウ酸尿 および hydrochlorothiazide   Oxalobacter formigenes 原発性シュウ酸尿 および Oxalobacter formigenes   Orthophosphate 原発性シュウ酸尿 および Orthophosphate   Magnesium oxide 原発性シュウ酸尿 および Magnesium oxide   pentosan polysulfate 原発性シュウ酸尿 および pentosan polysulfate 詳細については、ログインしてください、ログイン情報（クリックしてログインする）無料です ウェブ検索結果調査のための 原発性シュウ酸尿 ウェブ（すべて）  |  治療  |  薬  |  テスト  |  調査  |  ダイエット その結果 1 - 50 - 原発性シュウ酸尿 Primary hyperoxaluria - Wikipedia, the free encyclopedia 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 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 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 ... ... 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 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 ... 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. 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 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. 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 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. 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 ... ... 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. ... 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 ... ... 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 ... 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. 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 ... 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 ... ... 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 ... 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 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 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 ... 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 ... 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 ... 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 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 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 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 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 ... 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 ... 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 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 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 ... 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 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 ... 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 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 ... 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 ... ... 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 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 ... 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 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 ... 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 ... 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 ... 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 ... ... 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 ... 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 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 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 ... ... 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 ... ... 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 もっと表示 1  2