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Low-level laser therapy (LLLT) was cleared by the US Food and Drug Administration (FDA) for the treatment of lymphedema in November 2006. [63] According to the US National Cancer Institute, LLLT may be effective in reducing lymphedema in some women. Two cycles of laser treatment were found to reduce the volume of the affected arm in ...
This type of lymphedema usually develops as a result of a developmental abnormality being precipitated by some insult such as trauma, illness, or physical immobility. Compared to secondary lymphedema, primary lymphedema is more likely to involve the face, conjunctiva, and genitalia in association with any limbs involved. [2] It can be familial. [3]
It produces a mound, visible, firm and non-tender at the point of tactile stimulus approximately 1-2 seconds after stimulus, subsiding back to normal after 5-10 seconds. It is a sign in hypothyroid myopathy, such as Hoffmann syndrome. [7] In lymphedema, abnormal removal of interstitial fluid is caused by failure of the lymphatic system.
The Emberger syndrome is a rare, autosomal dominant, genetic disorder caused by familial or sporadic inactivating mutations in one of the two parental GATA2 genes. The mutation results in a haploinsufficiency (i.e. reduction) in the levels of the gene's product, the GATA2 transcription factor.
Lymphedema–distichiasis syndrome is a medical condition associated with the FOXC2 gene. [ 2 ] : 849 People with this hereditary condition have a double row of eyelashes , which is called distichiasis , and a risk of swollen limbs due to problems in the lymphatic system .
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