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Prolactin levels and gene polymorphism are not linked to vitiligo severity but are related to BMI.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

WNT10B is linked to cancer development and affects survival and disease progression in various cancers.

A baby had a unique skin condition with a pale patch and surrounding dark hairs, not linked to other health issues.

Higher levels of miR-203 may contribute to hair loss in alopecia areata.

People with Down's syndrome are more likely to have syringomas.

Different scalp and hair disorders are more common in certain ethnic groups, with the most common being androgenetic alopecia, which is treated with medications like minoxidil and finasteride.

A 45-year-old woman with autoimmune diseases experienced patchy hair loss due to alopecia areata, which has no cure but can be treated, with varying success.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

Androgens like testosterone affect skin health and can lead to conditions such as acne and hair loss, with various treatments available.

The conclusion is that adult males with muscle weakness and hormonal imbalances should be tested for Kennedy's disease.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

Men with early hair loss may have a higher risk of enlarged prostate and possibly prostate cancer due to shared hormonal factors.

No effective treatment exists to stimulate hair growth in atrichia with papular lesions.

Maintaining DNA integrity in stem cells is crucial to prevent aging and cancer.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

Nonclassic congenital adrenal hyperplasia is a common genetic disorder that can cause a range of symptoms and requires personalized treatment.

The 2004 hair research meeting presented new findings on hair cell differentiation, genetic factors in hair loss, hair pigmentation, and potential targeted therapies.

The Naked (N) trait in mice is linked to lower glycine and tyrosine in hair proteins.

Finasteride may effectively treat hair loss in Klinefelter Syndrome patients.

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

Testosterone metabolism in balding scalp cells may not be the main cause of hair loss.

The report concludes that PCOS is mainly a condition of excess male hormones and its definition may change as new information is discovered.

Experts agree that PCOS affects women's health in complex ways, but more research is needed to understand and treat it effectively.

PCOS is a complex condition with major health impacts, needing more research for better diagnosis and treatment.

Lgr5 is a marker for active, long-lasting stem cells in mouse hair follicles.

Chemotherapy in the first trimester of pregnancy is risky, but in the second and third trimesters, it's generally safe with careful drug selection and timing.

Different types of long-lasting stem cells are responsible for the growth and upkeep of the mammary gland.

Removing the ATR gene in adult mice causes rapid aging and stem cell loss.

Male hormones may play a role in the development of heart disease, and more research is needed to understand their effects.