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(Q84.1) Congenital morphological disturbances of hair, not elsewhere classified
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12 944 in individuals diagnosis congenital morphological disturbances of hair, not elsewhere classified confirmed
1 550 deaths with diagnosis congenital morphological disturbances of hair, not elsewhere classified
12% mortality rate associated with the disease congenital morphological disturbances of hair, not elsewhere classified
Diagnosis congenital morphological disturbances of hair, not elsewhere classified is diagnosed Men are 5.30% more likely than Women
6 815
Men receive the diagnosis congenital morphological disturbances of hair, not elsewhere classified
0 (less than 0.1%)Died from this diagnosis.
100
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6 129
Women receive the diagnosis congenital morphological disturbances of hair, not elsewhere classified
1 550 (25.3 %)Died from this diagnosis.
Risk Group for the Disease congenital morphological disturbances of hair, not elsewhere classified - Men and Women aged 0
In Men diagnosis is most often set at age 0-19, 25-34, 45-54
Less common in men the disease occurs at Age 20-24, 35-44, 55-95+Less common in women the disease occurs at Age 20-24, 55-59, 65-95+
In Women diagnosis is most often set at age 0-19, 25-54, 60-64
Disease Features congenital morphological disturbances of hair, not elsewhere classified
Absence or low individual and public risk
Congenital morphological disturbances of hair, not elsewhere classified - what does this mean
Congenital morphological disturbances of hair, not elsewhere classified, are a rare condition that is characterized by the presence of unusual hair structures from birth, such as abnormally thick, thin, or curly hair. these hair abnormalities can be caused by genetic mutations, environmental factors, or a combination of both.
What happens during the disease - congenital morphological disturbances of hair, not elsewhere classified
Congenital morphological disturbances of hair, not elsewhere classified, are caused by genetic mutations that interfere with the normal development of hair follicles and the structure of the hair itself. these mutations can manifest in a variety of ways, including abnormal hair texture, color, or thickness, as well as abnormalities in hair growth and shedding patterns. in some cases, these mutations can also cause alopecia, or hair loss.
Clinical Pattern
More details coming soon
How does a doctor diagnose
- Physical examination of the affected area
- Clinical history of the patient
- Laboratory tests such as blood tests, biopsy, and imaging studies
- Genetic testing
- Treatment with topical medications
- Surgery to correct the deformity
Treatment and Medical Assistance
Main goal of the treatment: To reduce the severity of the congenital morphological disturbances of hair, not elsewhere classified.
- Administering medications to reduce inflammation and itching.
- Prescribing topical treatments to reduce itching and inflammation.
- Prescribing oral medications to reduce inflammation and itching.
- Prescribing topical corticosteroids to reduce inflammation.
- Prescribing topical antifungal medications to reduce the risk of fungal infections.
- Prescribing oral antibiotics to reduce the risk of bacterial infections.
- Prescribing topical antihistamines to reduce itching.
- Performing scalp biopsies to diagnose the cause of the condition.
- Performing scalp treatments to reduce inflammation.
- Performing scalp surgery to correct anatomical abnormalities.
- Performing scalp laser therapy to reduce inflammation.
- Performing scalp massage to reduce itching.
- Recommending lifestyle changes to reduce stress and improve overall health.
9 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Congenital morphological disturbances of hair, not elsewhere classified - Prevention
The best way to prevent congenital morphological disturbances of hair is to ensure that pregnant women receive regular prenatal care and follow a healthy lifestyle. adequate nutrition, regular exercise, and avoiding exposure to environmental toxins can help reduce the risk of this condition.