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reduced results from
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51B options
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2M
reduced results due to: symptoms, possible diagnoses, age, gender
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364800
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 ?
false sense of muscle enlargement
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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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|paralysis|bodyache|muscle weakness in leg(s)|heart rate irregular|palpitations without fever|palpitations|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, palpitations, palpitations without fever, heart rate irregular, muscle weakness in leg(s), bodyache
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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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Hyperkalemic periodic paralysis - type of inherited genetic disorder
a.k.a HYPP, Impressive Syndrome, Gamstorp episodic adynamy
'hyperkalemic periodic paralysis' is considered a medical emergency
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Limb girdle muscular dystrophies - inherited diseases of muscle
a.k.a Erb's muscular dystrophy
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Facioscapulohumeral dystrophy - type of inherited muscle disease
a.k.a FSHMD, FSHD, FSH, Landouzy-Dejerine
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Spinal muscular atrophies types 2 and 3 - inherited disease causing muscle weakness
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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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Becker disease - rare inherited muscle disease
a.k.a Benign pseudohypertrophic muscular dystrophy
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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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Known synonyms for your symptoms:
• muscle pseudohypertrophy -
false appearance of increased muscle growth , false sense of muscle enlargement , apparent muscle enlargement
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