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TCDD speeds up skin barrier formation by increasing certain gene expressions.

The document concludes that early recognition and treatment of primary cicatricial alopecia is crucial to prevent permanent hair loss.

Understanding how hair follicle stem cells work can help find new ways to prevent hair loss and promote hair growth.

Thyroid hormone affects skin health, with too little causing rough, pale skin and too much leading to smooth, thin skin, and may also impact wound healing and skin conditions.

The HoVert technique is a simple, cost-effective new method that improves alopecia diagnosis by allowing detailed analysis from a single biopsy.

FAGA diagnosis uses blood tests and trichoscopy, with treatments like topical minoxidil, oral anti-androgens, and hormone-modulating drugs.

Hidradenitis suppurativa may be related to hormones and patients often have metabolic disorders; more research is needed to understand this connection.

The document concludes that better treatments for CCCA are needed and more research is required to understand its causes related to hairstyling and genetics.

Human hair has a protective lipid layer that can be damaged by moisture and treatments, affecting hair growth and health.

The document concludes that there are various treatments for different types of alopecia, but more research is needed for evidence-based treatments.

Some treatments work for common baldness, but there's less evidence for other hair loss types, and more research is needed.

The conclusion is that better understanding and more research are needed to effectively manage follicular and scarring disorders in skin of color, with an emphasis on patient education and cultural awareness.

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

Eyebrow loss has many causes and requires accurate diagnosis for proper treatment.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

The G60S Connexin43 mutation causes hair growth issues and poor hair quality in mice, similar to human ODDD patients.

A rare genetic skin condition usually affecting males was found in a 9-year-old girl.

Hormone imbalances can cause skin diseases, and understanding these links is important for diagnosis and treatment.

Topical therapies show promise for hair loss and acne treatment with minimal side effects.

Hair loss can indicate or worsen with systemic diseases, and treating the underlying condition is important.

Mice with too much sPLA₂-IIA have hair loss and poor wound healing due to abnormal hair growth and stem cell depletion.

Scarring hair loss found in female pattern; biopsy needed for diagnosis.

Long hair can cause hair loss due to constant pulling.

FAPD and possibly CCCA may be AGA subtypes, and treatments combining antiandrogens, hair growth agents, hair transplants, and anti-inflammatories could be effective.

Frontal Fibrosing Alopecia is a slowly progressing hair loss condition, likely underdiagnosed, with ineffective treatments, needing more research to understand it fully.

Diet affects baldness; eat balanced, less animal fat, more fruits, vegetables, and cereals.

A rare case of a woman having both lichen planus pigmentosus and classic lichen planopilaris at the same time.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

Folliculotropic mycosis fungoides has a worse prognosis than other types, with survival rates varying significantly based on subtype and organ involvement.

Repeated use of protein hair conditioner with heat or gamma irradiation can harm skin and hair health in rats.