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Hedgehog signaling helps keep hair follicle stem cells the same in both young and old human skin.

Early diagnosis and aggressive treatment are key for managing rare scalp disorders that cause permanent hair loss.

The position of the parietal whorl can predict safe donor areas for hair transplants in Korean men with male pattern baldness.

The document explains the genetic causes and characteristics of inherited hair disorders.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

Half of people with Alopecia Areata may see hair regrowth within a year without treatment, but recovery is unpredictable.

Mutant mice help researchers understand hair growth and related genetic factors.

Alopecia Areata is an autoimmune condition often starting before age 20, with varied treatment success and a need for personalized treatment plans.

Dermatoscopy is a useful tool for diagnosing hair disorders and can help choose samples for more detailed analysis.

Graft-versus-host disease is a complication where donor immune cells attack the recipient's body, often affecting the skin, liver, and gastrointestinal tract.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

The document concludes that surgery is a preferred treatment for cicatricial alopecia, with the method chosen based on individual factors and may require multiple sessions and careful postoperative care.

Mice lacking Insig proteins had hair growth problems due to cholesterol buildup, but this was fixed by the drug simvastatin.

Smoking harms skin health, causing slower wound healing, more wrinkles, and worsening some skin conditions, but may protect against certain others.

Androgen receptor signaling causes early aging of cells important for hair growth by damaging their DNA.

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

Hair and nails are similar keratin structures with different shapes and growth, affected by the same diseases and environmental factors.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

Various treatments exist for alopecia areata, but none are completely satisfactory; choice depends on age, disease extent, and preference.

New treatments for hair loss show promise but need more research to confirm safety and effectiveness.

Alopecia Areata is an autoimmune condition causing hair loss, influenced by genetics, environment, and possibly improved by anti-MIF therapy, with many patients experiencing regrowth within a year.

The most common cause of hair loss in children is tinea capitis, followed by alopecia areata and telogen effluvium.

The conclusion is that a more comprehensive and precise approach is needed for diagnosing PCOS to address its broader health risks.

New vitiligo treatments focus on controlling immune damage and restoring skin color.

A new keratin, hK6irs1, is found in all layers of the hair follicle's inner root sheath.

Basonuclin 2 is vital for the development of facial bones, hair follicles, and male germ cells in adult mice, and its absence can lead to dwarfism and abnormal follicles.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

Using animal names for skin conditions helps with learning and memory.

The protein FLCN is involved in cellular cleanup and is regulated by ULK1.

Recombinant cytokine therapy can cause skin reactions ranging from mild to severe.