The Fabry Disease The Fabry Disease Classification The Fabry Disease is a genetic disorder, caused by the lack of alphagalactosidase A. It is an x-linked recessive inheritance. Therefore it is the females that carry it. The ones who ar mostly affected by this distemper are the males. womanly carriers, though, may develop angiokeratomas and may have problems with burning pains. right sufficienty few of the carriers may also have kidney or core group total problems. This disease occurs in 1 of 40,000 people. Descriptions A individual with the Fabry disease develops angiokeratomas, which are clusters of raised, dot-like lesions.
Appearing during childhood or pubescence in the genital and thigh areas, these angiokeratomas increase in size and number. former(a) symptoms of this disease are burning pains in passel or feet, nausea, vomiting, abdominal pains, dizziness, headaches and generalized weakness. Swelling of the legs, caused by the throng of lymph, a yellowish body fluid, under...If you want to get a full essay, order it on our website:
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