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Definition for chylomicronemia syndrome

Chylomicronemia syndrome is an inherited disorder in which abnormal lipid (fat) metabolism causes chylomicrons (a type of lipids) to accumulate to massive levels in the blood.
http://www.nlm.nih.gov/medlineplus/ency/article/000405.htm


some common symptoms
impaired sensations
impaired sensations in arm(s)
impaired sensations in foot (feet)
impaired sensations in hand(s)


some related diagnoses
1 - 7 of 160 diagnoses
hyperventilation
hyperkalemic periodic paralysis
hypocalcemia
hyperkalemia
hypomagnesemia
Hyperlipoproteinemia Type III
diabetes mellitus type 2
  more

do i have 'chylomicronemia syndrome'?
In addition the following diagnostic tests might be need to help verify the diagnosis:



therapeutic procedures for 'chylomicronemia syndrome'?
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 chylomicronemia syndrome:





web search results for chylomicronemia syndrome
Results 1 - 50 - chylomicronemia syndrome
adam.about.com - summary
symptomnav.adam.com - summary
www.nlm.nih.gov - summary
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www.nlm.nih.gov - summary







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