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reduced results from
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89B options
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4M
reduced results due to: symptoms, possible diagnoses, age, gender
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633600
reduced results due to: duration, diagnostic tests, modifiers
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11
reduced results due to: first pass
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9
options
reduced results due to: final pass
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refinement options
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duration of symptoms:
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lifestyle modifiers
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ethnic background
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family history of
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1 - 9 of 9 diseases -
gender ?
age ?
myotonia
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score graph
The score graph represents the results on the x axis and the "score" on the y axis. The purpose of this graph is to visually display the relative scores and how dramatically or not the likelihood of the diseases compare.
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Show only results from category
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weighted category breakdown
This pie chart represents the results broken down categorically. The size of the pie, or "score" of the category, is the sum of the scores of the diseases in the category. Please note a disease may fall into multiple category.
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|heart rate irregular|palpitations with fever|difficulty breathing|muscle weakness in foot (feet)|LIFESTYLE - Family History|weakness|palpitations|LIFESTYLE - Ethnicity|bodyache|palpitations without fever|paralysis|DEMOGRAPHIC - age|DEMOGRAPHIC - duration|)
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variable sensitivity
This bar chart represents the variables that the results and their ordering are most sensitive too.
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The results should NOT be considered a diagnosis.
Please consult your health care provider.
edit important variables such as:
demo: duration, demo: age, paralysis, palpitations without fever, bodyache, life: Ethnicity, palpitations
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Periodic paralyses - genetic diseases causing recurrent episodes of paralysis
'periodic paralyses' is considered a medical emergency
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periodic paralyses
genetic or congenital, neurology, muscles
[acute and may recur]
bodyache, fatigue, muscle weakness in leg(s), weakness
Periodic paralysis is a group of rare genetic diseases that lead to weakness or paralysis (rarely death) from common triggers such as cold, heat, high carbohydrate meals, not eating, stress or excitement and physical activity of any kind.
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For associated diagnostic procedures and therapeutic solutions, click diagnosis for details.
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Malignant hyperthermia - life threatening reaction to certain drugs resulting in extremely high body temperature
a.k.a MH, MHS, malignant hyperthermia syndrome, malignant hyperpyrexia due to anaesthesia
'malignant hyperthermia' is considered a medical emergency
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Potassium-aggravated myotonia - genetic disorder affecting skeletal muscles
a.k.a Myotonia congenita (Na channel)
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Paramyotonia congenita - congenital disorder with inability to relax muscles
a.k.a PC, Paramyotonia congenita of von Eulenburg, Eulenburg disease
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Myotonic dystrophy - inherited multisystem disease
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myotonic dystrophy
eye diseases, genetic or congenital, neurology, muscles
[chronic with acute exacerbation]
muscle cramps in foot (feet), muscle weakness in leg(s), palpitations, weakness
Myotonic dystrophy (DM) is a chronic, slowly progressing, highly variable inherited multisystemic disease that can manifest at any age from birth to old age. It is characterized by a wasting of the muscles (muscular dystrophy), posterior subcapsular irridescent cataracts (opacity of the lens of the eyes), heart conduction defects, endocrine changes and myotonia (difficulty relaxing a muscle).
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For associated diagnostic procedures and therapeutic solutions, click diagnosis for details.
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Andersen-Tawil Syndrome - inherited long QT syndrome
a.k.a Andersen syndrome, Long QT syndrome 7
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Congenital myopathies - inherited muscle diseases
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Thomsen disease - rare muscle disease with inability to relax muscles
a.k.a myotonia congenita, myotonia congenita
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Becker disease - rare inherited muscle disease
a.k.a Benign pseudohypertrophic muscular dystrophy
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Known synonyms for your symptoms:
• difficulty relaxing muscles -
muscles are always tight , cannot relax muscles , unable to relax muscles , inability to relax muscles , myotonia , delayed muscle relaxation
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