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アルポート症候群 - 難聴遺伝的腎臓病
に定義されています アルポート症候群
Alport syndrome is a genetic condition characterized by the progressive loss of kidney function and hearing.
よりたくさんの
Alport syndrome is a genetic condition characterized by the progressive loss of kidney function and hearing. Alport syndrome can also affect the eyes. The presence of blood in the urine (hematuria) is almost always found in this condition.
It was first identified in a British family by Dr. Cecil A. Alport in 1927.
Wikipedia Feb 24 2007
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いくつかの共通の現象
難聴
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以下、通常よりも排尿
ビジョンの問題
いくつかの関連診断
1 - 7 of
110
診断
糖尿病のタイプ2
全身性エリテマトーデスerythematosis
網膜色素変性症
ループス腎炎
薬物や毒素
膜性糸球体腎炎
常染色体優性多発性嚢胞腎疾患
より
私はありますか? 'アルポート症候群'?
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 'アルポート症候群'
1 - 5 of
19
診断テスト
分子遺伝学的研究
アルポート症候群 および 分子遺伝学的研究
超音波検査は、尿管膀胱腎臓
アルポート症候群 および 超音波検査は、尿管膀胱腎臓
蛋白質とクレアチニンの24時間尿
excretion of protein and creatinine in 24 hour urine collection
アルポート症候群 および 蛋白質とクレアチニンの24時間尿
尿素
アルポート症候群 および 尿素
血、血小板数
Platelet Count
アルポート症候群 および 血、血小板数
包括的な目の試験を受けます
アルポート症候群 および 包括的な目の試験を受けます
クレアチニンクリアランス
アルポート症候群 および クレアチニンクリアランス
発達テスト
アルポート症候群 および 発達テスト
テストを聞いて
standard technique of representing hearing loss
アルポート症候群 および テストを聞いて
血清アルブミン
type of protein in human plasma
アルポート症候群 および 血清アルブミン
血清クレアチニン
アルポート症候群 および 血清クレアチニン
尿検査
Examination of urine to detect disease
アルポート症候群 および 尿検査
空腹時脂質プロファイル
アルポート症候群 および 空腹時脂質プロファイル
血清電解質
アルポート症候群 および 血清電解質
生検のスキンです
アルポート症候群 および 生検のスキンです
腎生検
アルポート症候群 および 腎生検
血小板形態
アルポート症候群 および 血小板形態
音声の受信しきい値のSRT
アルポート症候群 および 音声の受信しきい値のSRT
クレアチニンクリアランス
アルポート症候群 および クレアチニンクリアランス
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 'アルポート症候群'?
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 Alport's Syndrome:
治療の手順の検索結果 'アルポート症候群'
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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.
腎移植
アルポート症候群 および 腎移植
特殊教育
アルポート症候群 および 特殊教育
音声療法
アルポート症候群 および 音声療法
薬の検索結果 'アルポート症候群'
1 - 2 of
2
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.
ACE Inhibitors
アルポート症候群 および ACE Inhibitors
cyclosporine capsule
アルポート症候群 および cyclosporine capsule
ウェブ検索結果調査のための アルポート症候群
ウェブ(すべて)
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その結果
1 - 50
- Alport's Syndrome
Alport's syndrome
Alport's syndrome (AS) is a generalized inherited disorder of basement membranes, ... A, Seri M, De Marchi M Alport. syndrome with type I membranoproliferative ...
http://www.orpha.net/data/patho/GB/uk-alport.pdf
www.orpha.net
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summary
Glomerulonephritis (Nephritic Syndrome): Kidney Filtering Disorders ...
Another is hereditary nephritis (Alport's syndrome), a progressive disorder that ... Nephritis (Alport's Syndrome) Hereditary nephritis (Alport's syndrome) is ...
http://www.merck.com/mmhe/sec11/ch144/ch144b.html
www.merck.com
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summary
Alport's syndrome and diffuse leiomyomatosis
cells of the esophagus, are absent in leiomyomas from patients with Alport syndrome and diffuse ... Alport's syndrome, with proven COL4A5 gene. mutation, the ...
http://www.orpha.net/data/patho/GB/uk-leiomy.pdf
www.orpha.net
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summary
Alport syndrome
Alport syndrome is an inherited form of kidney inflammation (nephritis) ... Renal biopsy shows chronic glomerulonephritis with changes typical of Alport syndrome. ...
http://adam.about.com/encyclopedia/infectiousdiseases/Alport-syndrome.htm
adam.about.com
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summary
Alport syndrome - Wikipedia, the free encyclopedia
Diseases of the Kidney: Alport Syndrome ... "OMIM - ALPORT SYNDROME, AUTOSOMAL DOMINANT" ... Alport syndrome--clinical phenotypes, incidence, and pathology" ...
http://en.wikipedia.org/wiki/Alport_syndrome
en.wikipedia.org
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summary
Alport syndrome - Genetics Home Reference
Alport syndrome is a genetic condition characterized by the ... the COL4A3, COL4A4, and COL4A5 genes cause Alport syndrome. ... Alport syndrome ...
http://ghr.nlm.nih.gov/condition=alportsyndrome
ghr.nlm.nih.gov
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summary
Alport Syndrome - Yahoo! Health
Important It is possible that the main title of the report Alport Syndrome is not the name you expected. Please check the synonyms listing to find the alternate ...
http://health.yahoo.com/urinary-overview/alport-syndrome/hea...
health.yahoo.com
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summary
Alport syndrome
Genes and Disease provides an introduction to the relationship between genetic factors and human disease with a summary ... syndrome was named for Dr. Alport ...
http://www.ncbi.nlm.nih.gov/books/bv.fcgi?rid=gnd.section.263
www.ncbi.nlm.nih.gov
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summary
MedlinePlus Medical Encyclopedia: Alport syndrome
Alport syndrome is an inherited form of kidney inflammation (nephritis) ... Renal biopsy shows chronic glomerulonephritis with changes typical of Alport syndrome. ...
http://www.nlm.nih.gov/medlineplus/ency/article/000504.htm
www.nlm.nih.gov
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summary
Alport Syndrome
Important It is possible that the main title of the report Alport Syndrome is not the name you expected. Please check the synonyms listing to find the alternate ...
http://www.webmd.com/www/a-to-z-guides/Alport-Syndrome
www.webmd.com
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summary
Nephritic Syndrome: Glomerular Diseases: Merck Manual Professional
Nephritic syndrome is a manifestation of glomerular inflammation ... (Alport's Syndrome) ... Nephrotic syndrome occurs rarely. ...
http://www.merck.com/mmpe/sec17/ch235/ch235b.html
www.merck.com
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summary
Collagen IV-Related Nephropathies (Alport Syndrome and Thin Basement ...
Alport syndrome is characterized by renal, cochlear, and ocular involvement. ... Perimacular flecks occur in approximately 30% of individuals with Alport syndrome. ...
http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=alport
www.ncbi.nlm.nih.gov
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summary
Blood in urine (hematuria) - MayoClinic.com
Blood in urine (hematuria) â?" Comprehensive overview covers ... So can Alport syndrome, which affects the filtering membranes in the glomeruli of the kidneys. ...
http://www.mayoclinic.com/health/blood-in-urine/DS01013/METHOD=print
www.mayoclinic.com
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summary
IPEX (syndrome) - Wikipedia, the free encyclopedia
... transcarbamylase deficiency · Oculocerebrorenal syndrome ... Alport syndrome · Dent's disease · X-linked nephrogenic diabetes insipidus. No primary system ...
http://en.wikipedia.org/wiki/IPEX_(syndrome)
en.wikipedia.org
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summary
Alport syndrome - References - Genetics Home Reference
X-linked Alport syndrome: natural history and genotype-phenotype correlations in ... Distribution of type IV collagen in the cochlea in Alport syndrome. ...
http://ghr.nlm.nih.gov/condition=alportsyndrome/show/References
ghr.nlm.nih.gov
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summary
Collagen IV-Related Nephropathies (Alport Syndrome and Thin Basement ...
phenotypes from Alport syndrome to thin basement membrane nephropathy (TBMN). Subtypes of collagen IV-realted nephropathies are X-linked Alport syndrome (XLAS) ...
http://www.ncbi.nlm.nih.gov/bookshelf/picrender.fcgi?book=ge...
www.ncbi.nlm.nih.gov
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summary
Potter syndrome - Wikipedia, the free encyclopedia
3 Terminology: Syndrome vs. Sequence. 4 Classic form. 5 Normal ... Dent's disease - Alport syndrome. Ureter. Ectopic ureter - Megaureter. Pelvic. Bladder ...
http://en.wikipedia.org/wiki/Potter_syndrome
en.wikipedia.org
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summary
Index: NE: Merck Manual Home Edition
... That Can Cause Nephrotic Syndrome. hereditary (Alport's syndrome) ... (Nephritic Syndrome): Hereditary Nephritis (Alport's Syndrome) ... Syndrome ...
http://www.merck.com/mmhe/index/ind_ne.html
www.merck.com
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summary
Encyclopedia A-Az on Yahoo! Health
Health encyclopedia of diseases and conditions covering symptoms, definitions, alternative names, causes, incidence, ... Alport Syndrome. Alprazolam for PMS ...
http://health.yahoo.com/ency/healthwise/hw119898/hw119898-conres
health.yahoo.com
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summary
Ear, nose, and throat - Genetics Home Reference
congenital hereditary hematuria see Alport syndrome ... hereditary familial congenital hemorrhagic nephritis see Alport syndrome ...
http://ghr.nlm.nih.gov/conditionCategory=earnoseandthroat
ghr.nlm.nih.gov
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summary
Hearing Loss - Symptoms and Signs from MedicineNet
Information about hearing loss and communications disorders. Produced by our staff ... Alport Syndrome. Autoimmune Hearing Loss. Cogan's Syndrome. Head Trauma ...
http://www.medicinenet.com/hearing_loss/symptoms.htm
www.medicinenet.com
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summary
Stickler syndrome - Wikipedia, the free encyclopedia
Stickler syndrome is characterized by a distinctive facial appearance, eye ... COL3: Ehlers-Danlos syndrome, types 3&4 (Sack-Barabas syndrome) COL4: Alport syndrome ...
http://en.wikipedia.org/wiki/Stickler_syndrome
en.wikipedia.org
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summary
Isolated Hematuria: Approach to the Genitourinary Patient: Merck Manual ...
... such as IgA nephropathy, hereditary nephritis (Alport's syndrome), thin basement ... Loin pain?hematuria syndrome. Renal vein thrombosis. Thrombotic ...
http://www.merck.com/mmpe/print/sec17/ch226/ch226h.html
www.merck.com
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summary
203780
http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=203780
www.ncbi.nlm.nih.gov
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summary
Introduction: Glomerular Diseases: Merck Manual Professional
... · Nephritic and Nephrotic Syndromes· Nephritic Syndrome· Nephrotic Syndrome ... Alport's syndrome*, congenital nephrotic syndrome (Finnish type), corticosteroid ...
http://www.merck.com/mmpe/sec17/ch235/ch235a.html
www.merck.com
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summary
8154501
... membrane include Alport's syndrome (AS), nail-patella syndrome, and thin ... Nail-patella syndrome is characterized by nail dysplasia, patellar hypoplasia or ...
http://www.ncbi.nlm.nih.gov/pubmed/8154501
www.ncbi.nlm.nih.gov
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summary
Adam
Alport syndrome. Reflux nephropathy. Obstructive uropathy. More Features. Printer-friendly version ... Alport syndrome. Analgesic nephropathy ...
http://stvhs.adam.com/content.aspx?productId=101&pid=1&gid=000471
stvhs.adam.com
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summary
HEARING LOSS - Pedbase.org
Alport Syndrome. Treacher Collins Syndrome. Waardenburg Syndrome. 4. X-Linked Recessive. Alport Syndrome. Hunter Syndrome. 5. Mitochondrial Disorders. Kearns ...
http://www.pedbase.org/h/hearing-loss
www.pedbase.org
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summary
Orphanet: Alport syndrome
The portal for rare ... Alport syndrome. Orpha number. ORPHA63. Prevalence of rare diseases. 1-9 ... Alport syndrome (AS) is an inherited disease ...
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=63
www.orpha.net
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summary
Alport syndrome - OMIM - Genetic disorder catalog - Genetics Home Reference
... information in the Genetics Home Reference condition summary on Alport syndrome. ... Alport syndrome, autosomal dominant. OMIM topic: Alport syndrome, ...
http://ghr.nlm.nih.gov/condition=alportsyndrome/show/OMIM
ghr.nlm.nih.gov
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summary
Aicardi Syndrome - Wikipedia
Hyperlinked overview with history, epidemiology, pathophysiology, features, diagnosis, treatments, and prognosis.
http://en.wikipedia.org/wiki/Aicardi_syndrome
en.wikipedia.org
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summary
Buschke-Ollendorff syndrome - Wikipedia, the free encyclopedia
Buschke Ollendorff syndrome at NIH's Office of Rare ... COL4: Alport syndrome. COL5: Ehlers-Danlos syndrome, types 1&2 ... Goodpasture's syndrome. Laminopathy ...
http://en.wikipedia.org/wiki/Buschke-Ollendorff_syndrome
en.wikipedia.org
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summary
301050
http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=301050
www.ncbi.nlm.nih.gov
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summary
Index: GE: Merck Manual Home Edition
of Alport's syndrome. Glomerulonephritis (Nephritic Syndrome): Hereditary Nephritis ... Obesity and the Metabolic Syndrome: Genes. of polycystic kidney disease ...
http://www.merck.com/mmhe/index/ind_ge.html
www.merck.com
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summary
Conradi-Hünermann syndrome - Wikipedia, the free encyclopedia
FGFR2: Antley-Bixler syndrome ... Alport syndrome · Dent's disease · X-linked nephrogenic diabetes insipidus. No primary system ...
http://en.wikipedia.org/wiki/Conradi-H%C3%BCnermann_syndrome
en.wikipedia.org
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summary
Kidney Diseases - Genetics Home Reference
Alport syndrome. Birt-Hogg-Dubé syndrome. branchiootorenal syndrome. cystinosis. cystinuria ... renal coloboma syndrome. Townes-Brocks Syndrome ...
http://ghr.nlm.nih.gov/medlineplusTopic=kidneydiseases
ghr.nlm.nih.gov
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summary
Nephritic Syndrome: Glomerular Diseases: Merck Manual Professional
Also includes crescentic glomerulonephritis and chronic nephritic syndrome. ... Nephritic syndrome is a manifestation of glomerular ... (Alport's Syndrome) ...
http://www.merck.com/mmpe/sec17/ch235/ch235b.html?qt=nephritic+syndrome&alt=sh
www.merck.com
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summary
PMID 16970251
320-5 Alport's syndrome is a hereditary nephritis that may lead to end-stage ... We conclude that autosomal dominant Alport's syndrome, follows a rare mode of ...
http://www.ncbi.nlm.nih.gov/pubmed/16970251
www.ncbi.nlm.nih.gov
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summary
Ehlers-Danlos syndrome - Wikipedia, the free encyclopedia
Functional bowel disorders (functional gastritis, irritable bowel syndrome) ... COL3: Ehlers-Danlos syndrome, types 3&4 (Sack-Barabas syndrome) COL4: Alport syndrome ...
http://en.wikipedia.org/wiki/Ehlers_Danlos_Syndrome
en.wikipedia.org
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summary
Exner syndrome - Wikipedia, the free encyclopedia
Dent's disease - Alport syndrome. Ureter. Ectopic ureter - Megaureter. Pelvic. Bladder ... Hydatid cyst · Von Hippel-Lindau syndrome · Tuberous sclerosis ...
http://en.wikipedia.org/wiki/Exner_syndrome
en.wikipedia.org
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summary
Deafness and Related Topics
Trisomy 13 is a syndrome associated with the presence of a third ... syndrome ... Alport syndrome. Alport syndrome is an inherited disorder (usually X-linked) ...
http://adam.about.com/od/deafnessandrelatedtopics/
adam.about.com
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summary
Autosomal dominant Alport syndrome: molecular analysis of the COL4A4 ...
Autosomal dominant Alport syndrome: molecular analysis of the COL4A4 gene and ... BACKGROUND: Alport syndrome is a clinically and genetically heterogeneous ...
http://www.ncbi.nlm.nih.gov/pubmed/19129241?ordinalpos=6&ito...
www.ncbi.nlm.nih.gov
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summary
Marshall syndrome - Wikipedia, the free encyclopedia
Main article: Pierre Robin syndrome ... COL3: Ehlers-Danlos syndrome, types 3&4 (Sack-Barabas syndrome) COL4: Alport syndrome ...
http://en.wikipedia.org/wiki/Marshall_syndrome
en.wikipedia.org
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summary
Sack-Barabas syndrome - Wikipedia, the free encyclopedia
COL3: Ehlers-Danlos syndrome, types 3&4 (Sack-Barabas syndrome) COL4: Alport syndrome. COL5: Ehlers-Danlos syndrome, types 1&2 ...
http://en.wikipedia.org/wiki/Sack-Barabas_syndrome
en.wikipedia.org
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summary
COL4A3 - collagen, type IV, alpha 3 (Goodpasture antigen) - Genetics ...
Alport syndrome - caused by mutations in the COL4A3 gene. The autosomal recessive form of Alport syndrome results when two copies of the ...
http://ghr.nlm.nih.gov/gene=col4a3
ghr.nlm.nih.gov
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summary
Norton - ADAM
Search engine description ... Alport syndrome. Alström syndrome. Amelogenesis imperfecta. Anencephaly ... Toni-Fanconi syndrome. Deficiency - antithrombin III ...
http://nortonhealthcare.adam.com/content.aspx?productId=112&...
nortonhealthcare.adam.com
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summary
Approach to the Renal Patient: Approach to the Genitourinary Patient ...
... risk of polycystic kidney disease or hereditary nephropathy (Alport's syndrome) ... Occurs in acute tubular injury, glomerulonephritis, or nephrotic syndrome. WBC ...
http://www.merck.com/mmpe/print/sec17/ch226/ch226b.html
www.merck.com
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summary
Usher syndrome - Wikipedia, the free encyclopedia
This syndrome is characterized by deafness and a gradual vision loss. ... syndrome, including Alport syndrome, Alstrom syndrome, Bardet-Biedl syndrome, ...
http://en.wikipedia.org/wiki/Usher_syndrome
en.wikipedia.org
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summary
Search Results - Genetics Home Reference
Alport syndrome. Condition summary. Found: ...properly and ... Hearing loss is a common feature of Alport syndrome,... Related genes: COL4A3 COL4A4 COL4A5 ...
http://ghr.nlm.nih.gov/search?query=hearing+loss
ghr.nlm.nih.gov
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summary
MIM Morbid map
Alport syndrome, autosomal recessive, 203780 (3) COL4A3. 120070. 2q36-q37 ... Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis, 300194 (2) ...
http://www.ncbi.nlm.nih.gov/Omim/getmorbid.cgi?start=138
www.ncbi.nlm.nih.gov
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summary
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