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(L87.0) Keratosis follicularis et parafollicularis in cutem penetrans [kyrle]
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4 903 in individuals diagnosis keratosis follicularis et parafollicularis in cutem penetrans [kyrle] confirmed
Diagnosis keratosis follicularis et parafollicularis in cutem penetrans [kyrle] is diagnosed Men are 2.02% more likely than Women
2 501
Men receive the diagnosis keratosis follicularis et parafollicularis in cutem penetrans [kyrle]
0 (less than 0.1%)Died from this diagnosis.
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Women receive the diagnosis keratosis follicularis et parafollicularis in cutem penetrans [kyrle]
0 (less than 0.1%)Died from this diagnosis.
Risk Group for the Disease keratosis follicularis et parafollicularis in cutem penetrans [kyrle] - Men aged 70-74 and Women aged 85-89
In Men diagnosis is most often set at age 35-39, 45-59, 65-74, 80-84
Less common in men the disease occurs at Age 0-34, 40-44, 60-64, 75-79, 85-95+Less common in women the disease occurs at Age 0-9, 15-19, 25-29, 35-39, 45-49, 55-59, 65-79, 90-95+
In Women diagnosis is most often set at age 10-14, 20-24, 30-34, 40-44, 50-54, 60-64, 80-89
Disease Features keratosis follicularis et parafollicularis in cutem penetrans [kyrle]
Absence or low individual and public risk
Keratosis follicularis et parafollicularis in cutem penetrans [kyrle] - what does this mean
Keratosis follicularis et parafollicularis in cutem penetrans (kyrle) is a rare skin disorder characterized by the presence of keratotic follicular papules and parafollicular lesions. these lesions are usually localized on the lower extremities and may be associated with a variety of systemic symptoms, including fatigue, malaise, fever, and joint pain. the exact cause of this disorder is unknown, however, it is thought to be related to an immune-mediated process.
What happens during the disease - keratosis follicularis et parafollicularis in cutem penetrans [kyrle]
Keratosis follicularis et parafollicularis in cutem penetrans (kyrle) is a rare, chronic skin disorder caused by an accumulation of keratin (a protein) in the hair follicles and sweat glands of the skin. it is thought to be caused by a genetic mutation that results in an abnormal production of keratin, leading to a build-up of keratin in the affected areas. this build-up causes the skin to become scaly, thickened, and irritated. it can also cause itching, burning, and pain. other symptoms may include redness and swelling. treatment typically involves topical medications and lifestyle changes.
Clinical Pattern
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How does a doctor diagnose
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Treatment and Medical Assistance
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18 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Keratosis follicularis et parafollicularis in cutem penetrans [kyrle] - Prevention
Keratosis follicularis et parafollicularis in cutem penetrans [kyrle] is a rare skin disorder that can be prevented by avoiding sun exposure, using sunscreen with a high spf, wearing protective clothing when outdoors, and avoiding skin irritants. additionally, regular skin exams can help to identify any changes or areas of concern.