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Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.

Mice are useful for researching human hair loss and testing treatments, despite some differences between species.

Feed restriction in sheep leads to finer wool fibers but may reduce wool quality.

The conclusion is that formalizing how past decisions influence current health technology assessments could improve the credibility and defense of coverage decisions.

The research found specific signs to diagnose alopecia areata incognito and noted patients generally regrow hair after steroid treatment.

Madarosis is the loss of eyelashes and eyebrows due to various health issues and requires thorough examination to diagnose and treat the underlying cause.

Different factors help diagnose and treat hair loss accurately.

Signaling pathways are crucial for hair growth in goats.

With careful management, people with congenital adrenal hyperplasia can have successful pregnancies and become parents.

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

New skin substitutes for treating severe burns and chronic wounds are being developed, but a permanent solution for deep wounds is not yet available commercially.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

The document concludes that understanding hair follicles requires more research using computational methods and an integrative approach, considering the current limitations in hair treatment products.

Skin aging is caused by stem cell damage and can potentially be delayed with treatments like antioxidants and stem cell therapy.

The study found that Central Centrifugal Cicatricial Alopecia mainly affects middle-aged African descent women, is linked to certain hair care practices and genetics, and often goes undiagnosed for years.

Frontal Fibrosing Alopecia's cause is unclear, affects mainly postmenopausal women, and current treatments focus on stopping hair loss rather than regrowth.

People with myotonic dystrophy type 1 have a higher chance of getting skin tumors, including melanoma.

Trichoscopy helps tell apart scalp lesions in pemphigus vulgaris and pemphigus foliaceus and is useful for choosing biopsy locations.

Certain genetic variations in IL18 may increase the risk of alopecia areata in Koreans.

The conclusion is that skin and hair patterns are formed by a mix of cell activities, molecular signals, and environmental factors.

A genetic mutation caused severe rickets and alopecia in an Indian patient, but high-dose calcium and phosphate treatment improved their condition.

Skin patterns are formed by simple reaction-diffusion mechanisms.

The conclusion is that proper evaluation and treatment of hair loss in midlife women is important, considering the emotional impact and potential for various treatments.

In vivo lineage labelling is better than in vitro methods for identifying and understanding stem cells.

The document concludes that more research is needed to fully understand the causes of PCOS.

Genetic defects in the glucocorticoid receptor gene can cause conditions with abnormal sensitivity to stress hormones, and other factors may also affect this sensitivity.

Gene regulation could revolutionize hair color by altering pigmentation from within.

Epidermal stem cells create and maintain skin structures like hair and nails through specific signaling pathways and vary by location and function.

The document concludes that hormonal biomarkers are key for diagnosing hyperandrogenemia in women and hypogonadism in men.