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The safety and effectiveness of gender-affirming treatments for children are uncertain, with potential long-term risks like infertility.

A baby girl has a hair disorder called monilethrix, causing fragile hair that may improve over time.

The essay suggests hair loss might be caused by changes in skull bones.

A 12-year-old girl in Saudi Arabia with Focal dermal hypoplasia showed skin and dental symptoms, highlighting the condition's variability and the need for personalized treatment.

Genetic testing confirmed a rare skin disorder in a young girl, which improved with zinc supplementation.

Darier-White disease causes skin and nail issues, starts around age 20, worsens until 40-50, and has poor treatment options.

An 8-year-old girl has a rare genetic disorder causing complete, irreversible hair loss and skin bumps.

Hair follicle sampling is a feasible method to measure FMRP and FMR1 mRNA levels in children.

Two sisters have rare hair disorders causing short, fragile, kinky hair.

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.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

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.

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.