The Fabry Disease Classification The Fabry Disease is a hereditary disorder, caused by the lack A. It is an x-linked recessive inheritance. Therefore it is the females that carry it. The ones who are mostly affected by this disease are the males.
Female carriers, though, may develop and may have problems with burning pains. Very few of the carriers may also have kidney or heart problems. This disease occurs in 1 of 40, 000 people. Descriptions A person with the Fabry disease develops, which are clusters of raised, dot-like lesions. Appearing during childhood or puberty in the genital and thigh areas, these increase in size and number. Other symptoms of this disease are burning pains in hand or feet, nausea, vomiting, abdominal pains, dizziness, headaches and generalized weakness.
Swelling of the legs, caused by the gathering of lymph, a yellowish body fluid, under the skin may also occur. Skin will show telangiectasis, inflated intra-epidermal (intra – within, epidermal – outer layer) spaces filled with blood. Places (vessel wall) where there is no telangiectasis are filled with deposits of. These deposits are also found in the heart, muscles, renal tubules and glomeruli, central nervous system, spleen, liver, bone marrow, lymph nodes and cornea. Retarded growth, delayed puberty and ocular abnormalities are also common symptoms. These symptoms are mostly fond in males because they display full-blown syndrome, while females displays a partial form.
The Essay on Free Radicals Disease Body Symptoms
Communicable Diseases Disease 1: Hepatitis C Question 1 1. What are the symptoms? Symptoms for short term Hepatitis C may include mild cold symptoms, and fatigue. Long-term symptoms include: anorexia, nausea and jaundice. 2. How long does it last? 50% of people who are HCV positive overcome it in a few months. 10% to 15% may develop chronic liver disease over 10 - 20 years. 3. How is it treated? ...
Diagnosis They firsts take a urine sample, which is the first place where they would find anything. Then they would take a blood, bone marrow and ophthalmologic examination. Prenatal diagnosis by way of Amniocentesis or Chronic Villus Sampling is also available. Prognosis People affected by this disorder usually dies by the age of 40-50 from kidney failure or complications.
Treatment There is only treatment to relieve the pains of the symptoms. Researchers are working towards the possibility of replacing the enzyme. Bibliography The Encyclopedia of Genetic Disorder and Birth Defects, By JamesWynbrandt and Mark D. Ludman, M. D. , F.
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