Search your symptoms with MEDgle. You can check your symptoms. It is a medical symptom search allowing you find out what options make sense for you.
CLOSE
PATIENT GPS
患者
healthcare providers
how it works
約
ログイン
検索編集
新しい検索
症状が
診断
医師
薬
手順
close
症状が
診断
薬
手順
医師
symptom 持続
0から3日間
4月14日日
2週間-2ヶ月
2-6ヶ月
6ヶ月+
add symptom to current symptom search
上記と同じ
0から3日間
4月14日日
2週間-2ヶ月
2-6ヶ月
6ヶ月+
add symptom to current symptom search
上記と同じ
0から3日間
4月14日日
2週間-2ヶ月
2-6ヶ月
6ヶ月+
add symptom to current symptom search
上記と同じ
0から3日間
4月14日日
2週間-2ヶ月
2-6ヶ月
6ヶ月+
性別
男性
女性
年齢
1-3
4-11
12-17
18-29
30-50
50+
年齢
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
46
47
48
49
50
51
52
53
54
55
56
57
58
59
60
61
62
63
64
65
66
67
68
69
70
71
72
73
74
75
76
77
78
79
80
81
82
83
84
85
86
87
88
89
90
91
92
93
94
95
96
97
98
99
calculate
visual
[hide visual search]
search visually
症状が
|
診断
|
薬
|
手順
|
医師
検索の症状
•
あなたの症状の原因をして下さい
•
医師の発見関連タイプ
検索診断
•
診断の理解を見る
•
学ぶ関連検査や治療について
•
ウェブ上で有用なリソースをして下さい
検索薬
•
について学んで別の治療薬
•
理解何が使用されます
•
知っている可能性のオプション
search procedures
•
について学んで別の診断と治療の手順
•
理解何が使用されます
•
知っている可能性のオプション
検索の医師
•
お住まいの地域で医師をして下さい
•
理解彼らがありません
•
あなたが必要と右のヘルプを取得します
から減少の結果
8 B
1 M
177600
63
61
to ~6 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, 筋肉, neurology
周波数
珍しい (U.S.)
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
neurologist
adolescent medicine
genetics specialist
neurosurgeon
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.
先天性パラミオトニア - できない筋肉をリラックスすると先天性疾患
に定義されています 先天性パラミオトニア
Paramyotonia Congenita (PC), also known as Paramyotonia congenita of von Eulenburg or Eulenburg disease, is a rare congenital autosomal dominant neuromuscular disorder characterized by “paradoxical" myotonia.
よりたくさんの
Paramyotonia Congenita (PC), also known as Paramyotonia congenita of von Eulenburg or Eulenburg disease, is a rare congenital autosomal dominant neuromuscular disorder characterized by “paradoxical" myotonia. This type of myotonia has been termed paradoxical because it becomes worse with exercise whereas classical myotonia, as seen in myotonia congenita, is alleviated by exercise. PC is also distinguished as it can be induced by cold temperatures. Although more typical of the periodic paralytic disorders, patients with PC may also have potassium provoked paralysis. PC typically presents within the first decade of life and has 100% penetrance. Patients with this disorder commonly present with myotonia in the face or upper extremities. The lower extremities are generally less affected. While some other related disorders result in muscle atrophy, this is not normally the case with PC. This disease can also present as hyperkalemic periodic paralysis and there is debate as to whether the two disorders are actually distinct.
less
いくつかの共通の現象
活動に継続的な筋収縮
難易度リラックス筋肉
できない熟練の動きを実行します
筋硬直
いくつかの関連診断
1 - 5 of
5
診断
定期的に麻痺させる
カリウムはミオトニーを悪化させた
筋強直性ジストロフィー
アンデルセン- 258症候群
先天性myopathies
より
私はありますか? '先天性パラミオトニア'?
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 '先天性パラミオトニア'
1 - 3 of
3
診断テスト
分子遺伝学的研究
先天性パラミオトニア および 分子遺伝学的研究
筋電図筋電図
先天性パラミオトニア および 筋電図筋電図
筋生検
先天性パラミオトニア および 筋生検
治療の手順を '先天性パラミオトニア'?
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 paramyotonia congenita:
治療の手順の検索結果 '先天性パラミオトニア'
1 - 1 of
1
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.
ミオトニー要因をトリガしないでください
先天性パラミオトニア および ミオトニー要因をトリガしないでください
薬の検索結果 '先天性パラミオトニア'
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.
acetazolamide
先天性パラミオトニア および acetazolamide
mexiletine
先天性パラミオトニア および mexiletine
furosemide
先天性パラミオトニア および furosemide
paroxetine
先天性パラミオトニア および paroxetine
hydrochlorothiazide
先天性パラミオトニア および hydrochlorothiazide
Florinef
先天性パラミオトニア および Florinef
Hydrodiuril
先天性パラミオトニア および Hydrodiuril
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 先天性パラミオトニア
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
- 先天性パラミオトニア
Paramyotonia congenita - Wikipedia, the free encyclopedia
Paramyotonia congenita or hyperkalemic periodic paralysis? ... Paramyotonia congenita: genotype to phenotype correlations in two families and ...
http://en.wikipedia.org/wiki/Paramyotonia_congenita
en.wikipedia.org
-
summary
Paramyotonia congenita - Genetics Home Reference
Paramyotonia congenita is a disorder that affects muscles used for movement (skeletal muscles) ... This effect is dramatic in people with paramyotonia congenita. ...
http://ghr.nlm.nih.gov/condition=paramyotoniacongenita
ghr.nlm.nih.gov
-
summary
Paramyotonia congenita - References - Genetics Home Reference
... Genetics Home Reference condition summary on paramyotonia congenita. ... Tamaoka A. Paramyotonia congenita and skeletal sodium channelopathy. Intern Med. ...
http://www.ghr.nlm.nih.gov/condition=paramyotoniacongenita/show/References
www.ghr.nlm.nih.gov
-
summary
Distinguishing paramyotonia congenita and myotonia congenita by ...
Distinguishing paramyotonia congenita and myotonia congenita by electromyography. ... thenar muscles of two patients with paramyotonia congenita were compared with ...
http://www.ncbi.nlm.nih.gov/pubmed/6888415
www.ncbi.nlm.nih.gov
-
summary
Paramyotonia congenita - Related Gene(s) - Genetics Home Reference
Genetic Conditions > paramyotonia congenita > Related Gene(s) ... Lister Hill National Center for Biomedical Communications ... Department of Health & Human ...
http://ghr.nlm.nih.gov/condition=paramyotoniacongenita/show/Related+Gene(s)
ghr.nlm.nih.gov
-
summary
Paramyotonia congenita (von Eulenburg) in Denmark.
Paramyotonia congenita (von Eulenburg) in Denmark. Johnsen T, Friis ML. Paramyotonia congenita (von Eulenburg) (PMC) is described in a Danish family in ...
http://www.ncbi.nlm.nih.gov/pubmed/7395457
www.ncbi.nlm.nih.gov
-
summary
Paramyotonia congenita - Educational resources - Information pages ...
Genetic Conditions > paramyotonia congenita > Educational resources ... in the Genetics Home Reference condition summary on paramyotonia congenita. ...
http://ghr.nlm.nih.gov/condition=paramyotoniacongenita/show/...
ghr.nlm.nih.gov
-
summary
Paramyotonia congenita and hyperkalemic periodic paralysis map to the ...
Paramyotonia congenita and hyperkalemic periodic paralysis map to the same ... Paramyotonia congenita (PC), an autosomal dominant muscle disease, shares some ...
http://www.ncbi.nlm.nih.gov/pubmed/1654742
www.ncbi.nlm.nih.gov
-
summary
Paramyotonia congenita - Patient support - For patients and families ...
Genetic Conditions > paramyotonia congenita > Patient support - For patients ... in the Genetics Home Reference condition summary on paramyotonia congenita. ...
http://ghr.nlm.nih.gov/condition=paramyotoniacongenita/show/Patient+support
ghr.nlm.nih.gov
-
summary
Temperature-sensitive defects in paramyotonia congenita mutants R1448C ...
Temperature-sensitive defects in paramyotonia congenita mutants R1448C and T1313M. ... The biophysical origins of paramyotonia congenita and its exacerbation in cold ...
http://www.ncbi.nlm.nih.gov/pubmed/15318338?ordinalpos=7&ito...
www.ncbi.nlm.nih.gov
-
summary
Paramyotonia congenita or hyperkalemic periodic paralysis? Clinical and ...
1: Muscle Nerve. 1990 Jan;13(1):21-6. Paramyotonia congenita or hyperkalemic periodic paralysis? ... distinction between paramyotonia congenita (PC) and ...
http://www.ncbi.nlm.nih.gov/pubmed/2325698
www.ncbi.nlm.nih.gov
-
summary
Hyperkalemic periodic paralysis and paramyotonia congenita--a novel ...
1: J Neurol. 2001 Nov;248(11):1003-4. Hyperkalemic periodic paralysis and paramyotonia congenita--a novel sodium channel mutation. ...
http://www.ncbi.nlm.nih.gov/pubmed/11757950
www.ncbi.nlm.nih.gov
-
summary
Paramyotonia Congenita - Yahoo! Health
Important It is possible that the main title of the report Paramyotonia Congenita is not the name you expected. Please check the synonyms listing to find the ...
http://health.yahoo.com/children-resources/paramyotonia-cong...
health.yahoo.com
-
summary
Hyperkalemic periodic paralysis
It is one of a group of genetic disorders that includes hypokalemic periodic ... Paramyotonia congenita; Periodic paralysis - hyperkalemic. Causes ...
http://adam.about.com/encyclopedia/infectiousdiseases/Hyperk...
adam.about.com
-
summary
MedlinePlus Medical Encyclopedia: Hyperkalemic periodic paralysis
Paramyotonia congenita; Periodic paralysis - hyperkalemic. Definition Return to top. Hyperkalemic periodic paralysis is associated with elevated levels of potassium ...
http://www.nlm.nih.gov/medlineplus/ency/article/000316.htm
www.nlm.nih.gov
-
summary
Talk:Paramyotonia congenita - Wikipedia, the free encyclopedia
This is the talk page for discussing improvements to the Paramyotonia congenita article. ... edit · history · watch · refresh To-do list for Paramyotonia congenita: ...
http://en.wikipedia.org/wiki/Talk:Paramyotonia_congenita
en.wikipedia.org
-
summary
emailAFriend
Paramyotonia Congenita * Indicates required fields. From: Your Name:* Your Email Address: ... Clicking the send button signifies that you have read and agree ...
http://www.webmd.com/email_friend?chronicID=091e9c5e8001eca2
www.webmd.com
-
summary
Orphanet: Paramyotonia congenita of Von Eulenburg
The portal for rare diseases and orphan drugs ... Paramyotonia congenita of Von Eulenburg is characterised by exercise- or cold ...
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=EN&Expert=684
www.orpha.net
-
summary
Myotonia congenita - Wikipedia, the free encyclopedia
... disease · Neuromyotonia · Paramyotonia congenita. Congenital myopathy ... 3 · Generalized epilepsy with febrile seizures plus · Paramyotonia congenita ...
http://en.wikipedia.org/wiki/Myotonia_congenita
en.wikipedia.org
-
summary
MedlinePlus: Muscle Disorders
Genetics Home Reference: Paramyotonia congenita(National Library of Medicine) ... Arthrogryposis Multiplex Congenita (AMC)(American Association of Neuromuscular ...
http://www.nlm.nih.gov/medlineplus/muscledisorders.html
www.nlm.nih.gov
-
summary
WebMD Health A-Z - Find reliable health and medical information on ...
Find a comprehensive index of trusted health and medical information. It is your ultimate guide to reliable health ... Eulenburg Paramyotonia Congenita. von ...
http://www.webmd.com/a-to-z-guides/health-topics/vk-vo.htm
www.webmd.com
-
summary
Myopathies - Symptoms & Causes - neurologychannel
Although scientists know that certain myopathies are caused by genetic or glandular defects, for example, it is not ... and paramyotonia congenita. ...
http://www.neurologychannel.com/myopathies/causes.shtml
www.neurologychannel.com
-
summary
Encyclopedia P-Pz on Yahoo! Health
Health encyclopedia of diseases and conditions covering symptoms, definitions, alternative names, ... Paramyotonia Congenita. Paraplegia, Hereditary Spastic ...
http://health.yahoo.com/ency/p/
health.yahoo.com
-
summary
Congenital muscular dystrophy - Wikipedia, the free encyclopedia
Congenital ? dystrophin (Becker's, Duchenne) ? Distal ... · Myotonia congenita · Thomsen disease · Neuromyotonia · Paramyotonia congenita. Congenital myopathy ...
http://en.wikipedia.org/wiki/Congenital_muscular_dystrophy
en.wikipedia.org
-
summary
SCN4A - sodium channel, voltage-gated, type IV, alpha subunit ...
paramyotonia congenita - caused by mutations in the SCN4A gene ... episodes of muscle stiffness (myotonia) characteristic of paramyotonia congenita. ...
http://ghr.nlm.nih.gov/gene=scn4a
ghr.nlm.nih.gov
-
summary
Myotonia Congenita -- GeneReviews -- NCBI Bookshelf
Paramyotonia congenita, also termed paradoxical myotonia (muscle stiffness ... Individuals with paramyotonia congenita display extreme cold sensitivity, ...
http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=myotonia-c
www.ncbi.nlm.nih.gov
-
summary
Sodium channel mutations in acetazolamide-responsive myotonia congenita ...
... myotonia congenita, paramyotonia congenita, and hyperkalemic ... periodic paralysis (hyperKPP) and paramyotonia congenita (PC) are genetic muscle ...
http://www.ncbi.nlm.nih.gov/pubmed/8058156
www.ncbi.nlm.nih.gov
-
summary
Chromosome 17 - Conditions related to genes on chromosome 17 - Genetics ...
hereditary neuropathy with liability to pressure palsies ... pachyonychia congenita. paramyotonia congenita. Pompe disease. potassium-aggravated myotonia ...
http://ghr.nlm.nih.gov/chromosome=17/show/Conditions
ghr.nlm.nih.gov
-
summary
Charcot-Marie-Tooth disease - Wikipedia, the free encyclopedia
Congenital - dystrophin (Becker's, Duchenne) - Distal ... Myotonia congenita - Thomsen disease - Neuromyotonia - Paramyotonia congenita. Congenital myopathy ...
http://en.wikipedia.org/wiki/Charcot_Marie_Tooth_type_1_aplasia_cutis_congenita
en.wikipedia.org
-
summary
PubMed Link Image
Sodium channel mutations in paramyotonia congenita and hyperkalemic periodic paralysis. ... genetics Male Molecular Sequence Data Mutation Myotonia Congenita genetics ...
http://www.ncbi.nlm.nih.gov/pubmed/8388676
www.ncbi.nlm.nih.gov
-
summary
Potassium-aggravated myotonia - References - Genetics Home Reference
Colding-Jorgensen E, Duno M, Vissing J. Autosomal dominant monosymptomatic ... responsive myotonia congenita, paramyotonia congenita, and hyperkalemic periodic ...
http://ghr.nlm.nih.gov/condition=potassiumaggravatedmyotonia/show/References
ghr.nlm.nih.gov
-
summary
Hyperkalemic periodic paralysis
Hyperkalemic periodic paralysis is associated with elevated levels ... Paramyotonia congenita; Periodic paralysis - hyperkalemic. Symptoms: Weakness/paralysis ...
http://adam.about.com/encyclopedia/000316sym.htm
adam.about.com
-
summary
Neurologic Diseases - Genetics Home Reference
myotonia congenita. myotonic dystrophy. neurofibromatosis type 1 ... paramyotonia congenita. Parkinson disease. Pelizaeus-Merzbacher disease. Pendred syndrome ...
http://ghr.nlm.nih.gov/medlineplusTopic=neurologicdiseases
ghr.nlm.nih.gov
-
summary
Myotonia Congenita
Paramyotonia congenita, also termed paradoxical myotonia (muscle stiffness ... Conversely, in paramyotonia congenita, repeated muscle ...
http://www.ncbi.nlm.nih.gov/bookshelf/picrender.fcgi?book=ge...
www.ncbi.nlm.nih.gov
-
summary
Characterization of a new sodium channel mutation at arginine 1448 ...
1. Paramyotonia congenita is a temperature-sensitive skeletal muscle disorder ... of a new genetic mutation in a family with the paramyotonia congenita phenotype. ...
http://www.ncbi.nlm.nih.gov/pubmed/10381583
www.ncbi.nlm.nih.gov
-
summary
Mutation in the S4 segment of the adult skeletal sodium channel gene in ...
... skeletal sodium channel gene in an Italian paramyotonia congenita (PC) family. ... (as in the case of paramyotonia congenita, PC phenotype) or changes in ...
http://www.ncbi.nlm.nih.gov/pubmed/7721550?dopt=Abstract
www.ncbi.nlm.nih.gov
-
summary
Search Results - Genetics Home Reference
paramyotonia congenita. Condition summary. Found in name or synonym: Paralysis periodica ... myotonia congenita. Condition summary. Related term: periodic ...
http://ghr.nlm.nih.gov/ghr/search?query="Paralysis"&show=conditions
ghr.nlm.nih.gov
-
summary
Molecular and genetic characterisation of German families with ...
... of German families with paramyotonia congenita and demonstration of founder ... with a history of paramyotonia congenita (PC) were characterised by genetic ...
http://www.ncbi.nlm.nih.gov/pubmed/8005599
www.ncbi.nlm.nih.gov
-
summary
PMID 8619545
Paramyotonia congenita: the R1448P Na+ channel mutation in adult human skeletal muscle. ... current decay on paramyotonia congenita muscle compared to control ...
http://www.ncbi.nlm.nih.gov/pubmed/8619545
www.ncbi.nlm.nih.gov
-
summary
Search Results - Genetics Home Reference
paramyotonia congenita. Condition summary. Related classification: Myotonic Disorders ... Lister Hill National Center for Biomedical Communications ...
http://ghr.nlm.nih.gov/search?query="Myotonic+Disorders"
ghr.nlm.nih.gov
-
summary
Myopathies - Diagnosis - neurologychannel
Many times a myopathy is simply labeled nonspecific muscle myopathy because, ... It is especially helpful for diagnosing myotonia and paramyotonia congenita. ...
http://www.neurologychannel.com/myopathies/diagnosis.shtml
www.neurologychannel.com
-
summary
Hyperkalemic Periodic Paralysis Type 1 -- GeneReviews -- NCBI Bookshelf
Paramyotonia congenita. The cardinal symptom of paramyotonia ... and slow inactivation in paramyotonia congenita mutants expressed in Xenopus laevis oocytes. ...
http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=hyper-pp
www.ncbi.nlm.nih.gov
-
summary
Functional characterization and cold sensitivity of T1313A, a new ...
... of the skeletal muscle sodium channel causing paramyotonia congenita in humans. ... Paramyotonia congenita (PC) is a dominantly inherited skeletal muscle disorder ...
http://www.ncbi.nlm.nih.gov/pubmed/14617673
www.ncbi.nlm.nih.gov
-
summary
Bones, muscles, and connective tissues - Genetics Home Reference
Eulenburg Disease see paramyotonia congenita ... Von Eulenberg's disease see paramyotonia congenita. Vrolik disease see osteogenesis imperfecta ...
http://ghr.nlm.nih.gov/conditionCategory=bonesmusclesandconnectivetissues
ghr.nlm.nih.gov
-
summary
MedlinePlus Medical Encyclopedia: Topics beginning with P-Pl
Paramyotonia congenita see Hyperkalemic periodic paralysis ... Patent ductus arteriosus ligation see Congenital heart defect corrective surgeries ...
http://www.nlm.nih.gov/medlineplus/ency/encyclopedia_P-Pl.htm
www.nlm.nih.gov
-
summary
Accès au résumé PubMed / to PubMed abstract
... in a large cohort of UK patients with sodium channel paramyotonia congenita. ... cases met our core criteria for a clinical diagnosis of paramyotonia congenita. ...
http://www.ncbi.nlm.nih.gov/pubmed/18166706?ordinalpos=2&ito...
www.ncbi.nlm.nih.gov
-
summary
168300
http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=168300
www.ncbi.nlm.nih.gov
-
summary
Phenotypic variation of a Thr704Met mutation in skeletal sodium channel ...
... of both hyperkalaemic periodic paralysis and paramyotonia congenita. ... and electrophysiological characteristics of paralysis periodica paramyotonia. ...
http://www.ncbi.nlm.nih.gov/pubmed/11309455
www.ncbi.nlm.nih.gov
-
summary
Search Results - Genetics Home Reference
Found: Hypokalemic periodic paralysis is a condition ... paramyotonia congenita. Condition summary. Found in name or synonym: Paralysis periodica ...
http://ghr.nlm.nih.gov/search?query="Paralysis"
ghr.nlm.nih.gov
-
summary
Novel mutations in families with unusual and variable disorders of the ...
... have been described in paramyotonia congenita (PMC) and hyperkalaemic periodic paralysis (HPP) ... PMC, HPP and of a third disorder, myotonia congenita (MC) ...
http://www.ncbi.nlm.nih.gov/pubmed/1338909
www.ncbi.nlm.nih.gov
-
summary
もっと表示
1
2
よくある質問/約
|
免責事項
|
プライバシーポリシー
|
利用規約
|
ブラウズ
|
beta
|
お問い合わせ
|
API - Catalyst
MEDgle does not provide medical advice, diagnosis or treatment. Copyright 2006-2012, MEDgle Inc. All Rights Reserved. MEDgle is NOT affiliated with Google. Last Updated: Mar 14, 2012
This site complies to the
HONcode standard for trustworthy health
information:
verify here
.
Invited Sponsor for Communications Conference
Finalist -- search & reference
MEDgle 2009ビジネスアワードの医学研究でベストに選ばれています