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A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

The document concludes that more research is needed to understand excessive hair growth in women with normal hormone levels and regular ovulation.

Assessing newborn scalp hair can reveal important health information.

Accurate diagnosis is key for treating different kinds of hair loss, and immune response variations may affect the condition and treatment results.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

Early and personalized treatment for hair loss in young people is crucial to prevent permanent damage and should include psychological support.

A 5-year-old boy's skin condition improved with systemic valganciclovir after a cardiac transplant and immunosuppressive therapy.

Loose Anagen Syndrome is a hair condition where hairs can be easily pulled out, mainly affecting young girls, and may improve on its own or with treatment.

Some treatments like intralesional steroids and 5α-reductase inhibitors are effective for frontal fibrosing alopecia, but more research is needed.

Trichoscopy is a useful tool for diagnosing hair disorders without pulling out hair.

The document suggests that the traditional understanding of hair growth cycles and alopecia may be inaccurate and that blood supply plays a significant role in hair growth and loss.

The most common causes of hair loss in children in South-East Nigeria are fungal infections and alopecia areata.

Topical minoxidil effectively and safely treats extensive alopecia areata but doesn't change its course.

Some congenital hair disorders improve in childhood or with treatments like minoxidil and retinoids, while others like Netherton syndrome and trichothiodystrophy have a poor prognosis.

Minoxidil helps treat eyebrow thinning, monilethrix, early hair loss, and shortens chemo-related hair loss.

New hair and skin changes were found in a rare case of syphilis-related hair loss.

Certain leukemia drugs can cause severe skin reactions that may require stopping treatment.

New hair transplant methods offer more natural results and better graft survival, with ongoing research to increase donor hair options.

KFSD is a genetic disorder causing hair loss and skin issues, with no effective treatment.

Some breast cancer patients developed permanent hair loss after chemotherapy and hormonal therapy, showing patterns similar to common baldness and alopecia areata.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

The most common causes of hair loss in Jordanian children are fungal infections, autoimmune hair loss, and hair shedding after fever, with zinc deficiency also being a notable cause.

The conclusion is that the best approach for treating Female Pattern Hair Loss is a combination of different treatments.

Most hair loss in children is caused by a few common conditions, and it's important to diagnose these properly and support the child's mental health.

Diagnosing hair loss disorders needs clinical, dermoscopic, and histological differences, and checking menstrual cycle, weight changes, drug therapy, and nail changes.

Corticosteroids may effectively regrow hair in Alopecia Totalis with manageable side effects.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

Cholesterol balance is important for hair health, and problems with it can lead to hair loss conditions.

Many skin patients also have mental health issues, and doctors should treat both together.