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The results should NOT be considered a diagnosis.
Please consult your health care provider.
edit important variables such as:
muscle weakness in foot (feet), impaired sensations in foot (feet), rash on arm(s), demo: duration, life: High Fat Diet, life: Obesity, life: Sedentary
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Compartment syndrome - increased pressure within a confined space causing tissue death
a.k.a problem with recent cast
'compartment syndrome' is considered a medical emergency
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Iliofemoral arterial occlusion - obstruction of iliac and femoral arteries
'iliofemoral arterial occlusion' is considered a medical emergency
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Hypertension - high blood pressure
a.k.a high blood pressure, HTN, HPN, essential hypertension, elevated blood pressure
'hypertension' is considered a medical emergency
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Hyperlipidemia
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Aortic aneurysm - rupture of bulge in wall of aorta
a.k.a ruptured aortic aneurysm, ruptured aneurysm of the aorta, ruptured aortic aneurysm
'aortic aneurysm' is considered a medical emergency
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aortic aneurysm
cardiac, vascular problems
[chronic]
pain in back, palpitations, stomach pain, upper abdominal pain
An aortic aneurysm is a general term for any swelling (dilatation or aneurysm) of the aorta, usually representing an underlying weakness in the wall of the aorta at that location. While the stretched vessel may occasionally cause discomfort, a greater concern is the risk of rupture which causes severe pain, massive internal hemorrhage and, without prompt treatment, results in a quick death.
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For associated diagnostic procedures and therapeutic solutions, click diagnosis for details.
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Homocystinuria - multisystem metabolic disease due to abnormal methionine metabolism
a.k.a Cystathionine beta synthase deficiency
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homocystinuria
cardiovascular, genetic or congenital, hematological, metabolic, muscles, musculoskeletal and connective tissue disorders, neurological
[chronic]
anemia, curvature of spine, delayed development, pain in leg(s)
Homocystinuria, also known as Cystathionine beta synthase deficiency, is an inherited disorder of the metabolism of the amino acid methionine. It is an inherited autosomal recessive trait, which means a child needs to inherit the defective gene from both parents to be affected.
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For associated diagnostic procedures and therapeutic solutions, click diagnosis for details.
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Hypercholesterolemia,
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Known synonyms for your symptoms:
• absent or diminished popliteal pulses -
decreased or absent pulses behind knee , decreased or absent popliteal artery pulses
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