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Scientists have made progress in understanding hair follicle stem cells, identifying specific genes and markers, and suggesting their use in treating hair and skin conditions.

Primary health care in Florianópolis mostly treated simple skin conditions, while secondary care handled more complex skin diseases.

Early treatment of children's hair loss, which can be caused by various factors, is important due to its emotional impact.

Transfollicular drug delivery is promising but needs more research to improve and understand it better.

Androgenetic alopecia causes hair thinning due to increased androgen activity, treatable with minoxidil and finasteride.

LC-OCT helps accurately diagnose different types of infant hair loss without invasive methods.

Trichoscopy helps accurately diagnose Netherton syndrome, often mistaken for atopic dermatitis.

Hair from the head was successfully used to restore pubic hair, with additional procedures suggested for more natural results.

Women with nonclassic congenital adrenal hyperplasia experience more sexual dysfunction and distress.

A patient with Rothmund-Thomson syndrome showed skin changes, hair loss, and dental defects but no cataracts or skeletal issues.

Excess male hormones in postmenopausal women can cause health issues and increase the risk of heart disease and diabetes; treatment depends on the cause.

Diabetes can lead to blindness and skin problems, and managing blood sugar and blood pressure is crucial to prevent these complications.

Tissue expanders effectively repair large scalp defects and restore a natural-looking scalp.

Congenital triangular alopecia can occur outside the typical fronto-temporal region.

Understanding the normal hair cycle and different types of hair loss is important for maintaining healthy hair.

A calf in Scotland likely had Schmallenberg virus from its mother.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

Adults with classic congenital adrenal hyperplasia value medication that prevents weight gain from glucocorticoids the most.

New hair regrowth model proposed, imiquimod found to kill skin cancer cells, T-cadherin loss linked to invasive skin cancer, no clear gene link to skin cancer after transplant, and study on children's hair loss shows male dominance and genetic ties.

A girl with a rare skin condition called Keratosis Follicularis Spinulosa Decalvans showed no significant improvement with treatment.

An American Bully with a genetic skin condition improved significantly with specific topical treatments.

Drug repositioning offers hope for new, affordable treatments for a genetic skin disorder called ARCI.

The fuzzy gene is crucial for controlling hair growth cycles.

Topical ceramide treatment partially improves the skin condition in Jack Russell Terriers with a genetic skin disorder.

The chapter explains that there are many genetic skin disorders affecting skin cell formation, including both common and rare types.

A 3-year-old girl with skin mast cell buildup and congenital baldness improved with treatment, suggesting a rare link between these conditions.

The hr gene is crucial for skin and hair health, with mutations causing hair disorders.

Trichoscopy is useful for diagnosing hair and scalp disorders in people with darker skin.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.