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Encyclopedia of Health and Medicine

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azotemia 177<br />

early childhood, typically following an upper respiratory<br />

viral INFECTION such as a cold. As the damage<br />

to the kidneys progresses, symptoms exp<strong>and</strong> to<br />

include ALBUMINURIA (excessive albumin or protein<br />

in the urine) <strong>and</strong> HYPERTENSION (high BLOOD PRES-<br />

SURE). About 80 percent <strong>of</strong> those who have Alport’s<br />

syndrome develop neurosensory HEARING LOSS by<br />

ADOLESCENCE, <strong>and</strong> 15 percent have irregularities in<br />

the shape <strong>of</strong> the lens <strong>of</strong> the eye (lenticonus).<br />

Symptoms in combination with family history<br />

strongly suggest Alport’s syndrome, though kidney<br />

biopsy is the definitive diagnostic tool. Kidney<br />

biopsy, in which the urologist extracts a core <strong>of</strong><br />

kidney tissue using a large-gauge needle, allows<br />

the him or her to determine the absence <strong>of</strong> any <strong>of</strong><br />

the three affected protein chains as well as to<br />

assess the degree <strong>of</strong> damage already present. SKIN<br />

biopsy can confirm X-linked Alport’s syndrome<br />

because the skin in this type <strong>of</strong> the disorder lacks<br />

the alpha-5 protein chain.<br />

Treatment Options <strong>and</strong> Outlook<br />

Treatment is primarily supportive <strong>and</strong> targets<br />

symptoms such as hypertension, hearing loss, <strong>and</strong><br />

VISION IMPAIRMENT. For people who reach ESRD,<br />

KIDNEY TRANSPLANTATION <strong>of</strong>ten <strong>of</strong>fers a viable therapeutic<br />

course. With treatment, many people who<br />

have Alport’s syndrome are able to enjoy the<br />

lifestyles <strong>of</strong> their choosing well into the fifth or<br />

sixth decade <strong>of</strong> life. The likelihood <strong>of</strong> RENAL FAILURE<br />

increases with age, however.<br />

Risk Factors <strong>and</strong> Preventive Measures<br />

Because Alport’s syndrome is an inherited genetic<br />

disorder, the only risks for this condition are the<br />

causative gene mutations. There are no measures<br />

to prevent the condition. Early treatment for consequential<br />

health conditions <strong>and</strong> close medical<br />

monitoring <strong>of</strong> kidney function help maintain optimal<br />

health.<br />

See also ALVEOLUS; GENETIC DISORDERS; GLOMERU-<br />

LUS; INHERITANCE PATTERNS; MUTATION; RENAL DIALYSIS.<br />

anuria The failure to produce URINE. Numerous<br />

circumstances can result in anuria, from severe<br />

DEHYDRATION <strong>and</strong> severe HYPOTENSION (low BLOOD<br />

PRESSURE) to END-STAGE RENAL DISEASE (ESRD) <strong>and</strong><br />

RENAL FAILURE. Anuria requires prompt medical<br />

evaluation to determine <strong>and</strong> remedy the underlying<br />

cause. Without such correction, waste byproducts<br />

accumulate to toxic levels <strong>and</strong> the body<br />

cannot continue to function.<br />

See also DYSURIA; ENURESIS; NOCTURIA; OLIGURIA;<br />

URINARY INCONTINENCE.<br />

azotemia<br />

See UREMIA.

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