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
patients
healthcare providers
how it works
about
login
edit search
new search
symptoms
diagnoses
physicians
drugs
procedures
close
symptoms
diagnoses
drugs
procedures
physicians
symptom duration
0-3 days
4-14 days
2 weeks-2 months
2-6 months
6 months +
add symptom to current symptom search
same as above
0-3 days
4-14 days
2 weeks-2 months
2-6 months
6 months +
add symptom to current symptom search
same as above
0-3 days
4-14 days
2 weeks-2 months
2-6 months
6 months +
add symptom to current symptom search
same as above
0-3 days
4-14 days
2 weeks-2 months
2-6 months
6 months +
gender
male
female
age
1-3
4-11
12-17
18-29
30-50
50+
age
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
symptoms
|
diagnoses
|
drugs
|
procedures
|
physicians
search symptoms
•
Find causes for your symptoms
•
Discover relevant types of physicians
search diagnoses
•
Understand the details of a diagnosis
•
Learn about relevant tests and treatments
•
Find useful resources on the web
search drugs
•
Learn about different therapeutic drugs
•
Understand what they are used for
•
Know the potential options
search procedures
•
Learn about different diagnostic and therapeutic procedures
•
Understand what they are used for
•
Know the potential options
search physicians
•
Find physicians in your area
•
Understand what they do
•
Get the right help you need
reduced results from
8 B
1 M
177600
63
61
to ~6 options
options split into images, definition, symptoms, related diagnoses, diagnostic tests, therapies, and medications
category
genetic or congenital, muscles, neurology
frequency
rare (U.S.)
likelihood by age
likelyhood by duration of symptoms
related physician types
family practitioner
internist
neurologist
adolescent medicine
genetics specialist
neurosurgeon
postal code
Find Local
The results are computer generated suggestions to help you find a physician. MEDgle does not recommend any particular type of physician or claim to be complete or accurate in the providers and specialties suggested.
paramyotonia congenita - congenital disorder with inability to relax muscles
Definition for paramyotonia congenita
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.
more
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
some common symptoms
continuous muscle contractions with activity
difficulty relaxing muscles
inability to perform skilled movements
muscle rigidity
some related diagnoses
1 - 5 of
5
diagnoses
periodic paralyses
potassium-aggravated myotonia
myotonic dystrophy
Andersen-Tawil Syndrome
congenital myopathies
more
do i have 'paramyotonia congenita'?
In addition the following diagnostic tests might be need to help verify the diagnosis:
diagnostic test search results for 'paramyotonia congenita'
1 - 3 of
3
diagnostic tests
Molecular Genetic Studies
paramyotonia congenita and Molecular Genetic Studies
Electromyogram (EMG)
paramyotonia congenita and Electromyogram (EMG)
Muscle biopsy
paramyotonia congenita and Muscle biopsy
therapeutic procedures for 'paramyotonia congenita'?
Managing or treating a diseases should always be determined by a patients health care provider. Below is a list of associated therapeutic procedures or medications for paramyotonia congenita:
therapeutic procedure search results for 'paramyotonia congenita'
1 - 1 of
1
therapeutic procedures
rankings are computer generated. please consult your health care provider.
avoid myotonia triggering factors
paramyotonia congenita and avoid myotonia triggering factors
medications search results for 'paramyotonia congenita'
1 - 5 of
7
medications
rankings are computer generated. please consult your health care provider.
acetazolamide
paramyotonia congenita and acetazolamide
mexiletine
paramyotonia congenita and mexiletine
furosemide
paramyotonia congenita and furosemide
paroxetine
paramyotonia congenita and paroxetine
hydrochlorothiazide
paramyotonia congenita and hydrochlorothiazide
Florinef
paramyotonia congenita and Florinef
Hydrodiuril
paramyotonia congenita and Hydrodiuril
for more please login, login is free (click to login)
web search results for paramyotonia congenita
Web (All)
|
Treatment
|
Drugs
|
Tests
|
Research
|
Diet
Results
1 - 50
- paramyotonia congenita
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
show more
1
2
faq/about
|
disclaimer
|
privacy policy
|
terms of service
|
browse
|
beta
|
contact
|
API - Catalyst
MEDgle does not provide medical advice, diagnosis or treatment. Copyright 2006-2011, MEDgle Inc. All Rights Reserved. MEDgle is NOT affiliated with Google. Last Updated: July 24, 2011
This site complies to the
HONcode standard for trustworthy health
information:
verify here
.
Invited Sponsor for Communications Conference
Finalist -- search & reference
MEDgle has been selected for the 2009 Best of Business Award in the Medical research
Featured Partners:
SEO Services
,
Search Engine Marketing
,
Parenting & Baby Information