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Kennedy's disease leads to muscle weakness and sensory issues, has no cure but manageable symptoms, and future treatments look promising.

Hairless protein is crucial for healthy skin and hair, and its malfunction can cause hair loss.

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

The document concludes that Rabson-Mendenhall syndrome requires novel treatments for insulin resistance and emphasizes the importance of dental care in affected patients.

Minoxidil treatment improves heart defects in a DiGeorge syndrome model.

The Hairless gene is crucial for healthy skin and hair growth.

The guideline recommends mental health involvement in diagnosing gender identity disorder and outlines hormone and surgical treatment protocols, emphasizing safety, informed consent, and long-term monitoring.

Zinc can both inhibit and stimulate mouse hair growth, and might help recover hair after chemotherapy.

Defective mitochondrial DNA replication causes aging symptoms and increased oxidative damage in mice.

Human enzymes can detoxify harmful substances but might also increase their cancer risk.

The document concludes that careful design of genetic fate mapping experiments is crucial for accurate cell lineage tracing in mice.

Certain transcription factors are key in controlling skin stem cell behavior and could impact future treatments for skin repair and hair loss.

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

The guide helps doctors diagnose hair problems by suggesting a thorough patient history, physical exams, and various diagnostic tools.

Different light affects cell functions and can help treat skin conditions.

Tacrolimus causes fewer acute rejections than cyclosporin A in kidney transplants but doesn't necessarily improve kidney function after one year; cardiovascular risks and side effects vary between the two drugs.

The meeting discussed vitamin D3's role in fighting tuberculosis, potential treatments for skin conditions like psoriasis, and hair follicle regeneration as a possible solution for hair loss.

The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

Atopic dermatitis may have genetic causes and can be treated with pharmacologic methods, glycerin creams, and controlling Staphylococcus aureus colonization.

Vitamin D affects Msx1 protein expression and may influence mineralized tissue health.

B6.Cg-Tyr c−2J Hr hr /J mice have a stronger delayed sunburn reaction and are good for UV research.

Altering SSAT affects fat metabolism and body fat in mice.

Sox21 is crucial for tooth development and enamel formation by preventing cells from changing into a different type.

The protein p53 directly reduces the production of Keratin 17, a skin and hair protein, in rats with radiation dermatitis.

Knocking out certain genes in mice helps understand skin and hair growth problems.

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

Long-term use of difluprednate eye drops in dogs can lead to hair loss and hormone imbalance.

People with hypohidrotic ectodermal dysplasia are more likely to experience long-term fatigue and hair loss after COVID-19.

Metreleptin treatment significantly improved metabolic health in a boy with congenital generalized lipodystrophy.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.