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Pioglitazone usually doesn't effectively treat or cure lichen planopilaris.

FGF13 gene changes cause excessive hair growth in a rare condition.

The document concludes that early diagnosis and treatment are key for pediatric hair loss disorders, and addressing the emotional effects on children is important.

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

Some diseases can improve the outcomes of other diseases, leading to new treatment possibilities.

The document concludes that alopecia has significant social and psychological effects, leading to a market for hair loss treatments.

Dermatologists are crucial for managing skin side effects in metastatic melanoma patients using vemurafenib and ipilimumab.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

The dermal papilla is crucial for hair growth and health, and understanding it could lead to new hair loss treatments.

Malt1 protease is essential for regulatory T cell function and could be targeted to boost antitumor immunity.

Different types of skin cells have unique genetic markers that affect how likely they are to spread cancer.

Beige and leaden pigment genes act within melanocytes, affecting pigment patterns.

Melatonin directly affects mouse hair follicles and may influence hair growth.

Lrig1 could be a marker for advanced sebaceous carcinoma.

Blood removal and birth control pills both helped with hormone levels in women with PCOS, but birth control was better for regular periods and blood removal had fewer side effects.

Gamma rays did not change hair follicle density but increased white and hypopigmented hairs in mice.

Apremilast was not effective in treating moderate-to-severe alopecia areata.

Mutations in the CYP21A2 gene are not a major factor in causing PCOS.

Skin may help in getting rid of excess iron through the process of skin cell renewal.

Low selenium levels can extend lifespan but worsen health issues.

Hair loss in mice starts with immune cells damaging hair roots before it becomes visible.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

IL-2 treatment causes skin eruptions and other reversible side effects, and may play a role in psoriasis.

FOXN1 mutations cause severe immunodeficiency, hair loss, nail issues, and thymus defects.

HSP90 and lamin A/C are crucial for hair growth and could be targets for treating hair loss.

BMAL1 controls skin cell growth and UV damage risk, peaking at night.

Alopecia areata caused a boy's hair to regrow straight instead of curly, but the exact reason is unknown.

Estrogens are key for bone growth spurts in both boys and girls and affect growth into adulthood.

Genes related to keratin, skin cell differentiation, and immune functions are key in hedgehog skin and spine development.

The guidelines help doctors manage skin problems from certain cancer treatments to improve patients' lives.