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Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

Puberty involves complex hormonal changes, varies by gender and ethnicity, and requires careful monitoring for abnormalities.

The document concludes that lifestyle changes and medical treatments can significantly reduce symptoms of Hidradenitis Suppurativa, a chronic skin condition.

The dataset includes detailed genetic information from mouse skin cells before and after injury.

The dataset includes detailed genetic information from mouse skin cells before and after injury.

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

Hair loss in certain mice is linked to changes in keratin-related genes.

The mouse hairy ears mutation causes longer ear hair due to changes in gene expression.

An 11-year-old child with total hair loss may have a genetic autoimmune disease, and the outlook for hair regrowth is not good.

The document concludes that Cutaneous Lupus Erythematosus has different forms, is influenced by genetic and environmental factors, and can be treated with various medications, but more targeted therapies are needed.

Insulin resistance and obesity are key factors in the development and worsening of polycystic ovary syndrome, and lifestyle changes are important for managing it.

PCOS may start before birth, involves metabolic issues, and can be treated with drugs like metformin and lifestyle changes.

Activating β-catenin in mammary cells leads to changes that cause early-stage abnormal growths similar to skin structures.

Environmental factors like smoking, UV exposure, and poor diet contribute to hair loss and graying, and lifestyle changes can help manage it.

Androgenic alopecia, a common hair loss condition, is linked to changes in androgen metabolism and genetics, and can be treated with finasteride and minoxidil, but these treatments are only fully effective in 10% of patients.

Androgens affect hair growth and shedding, with genetic and non-genetic factors influencing baldness.

Changes in skin microbes play a role in some skin diseases and could lead to new treatments.

A boy's hair that was frizzy and hard to comb returned to normal after 9 months, possibly due to genetic factors.

A teenager's hair with alternating white and dark bands, known as Pili annulati, is a genetic condition that is usually harmless and often considered attractive.

The project aimed to understand how genetic test results affect patients' actions and feelings in dermatology.

Skin problems in the elderly are unique and may indicate other diseases, involving changes in skin, hair, nails, and increased cancer risk.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

Alopecia areata is likely caused by a combination of genetic factors and immune system dysfunction, and may represent different diseases with various causes.

Hair loss treatments work better with lifestyle changes.

Genes and epigenetic changes are important in the development of Polycystic Ovary Syndrome.

Changes in NRF2 levels may contribute to hair loss in Egyptian men.

The conclusion is that genetic differences affect how the cochlea heals after hair cell loss, which may challenge the creation of hearing loss treatments.

Different hair types in mammals are linked to variations in specific protein genes, with changes influenced by their living environments.

Hair gets thinner, grayer, and changes texture with age due to genetics, environment, and cellular changes, affecting the growth cycle.

Ingenol mebutate gel changes gene expression related to skin development and immune response in actinic keratosis.