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Steroid Sulfatase inhibitors show promise in treating hormone-dependent disorders like cancers, hair loss, and acne, with 667COUMATE being a potential candidate for breast cancer treatment trials.

The review shows how to properly diagnose and treat the loss of eyebrow and eyelash hair.

Dermatologists diagnose and manage melanoma more effectively than general practitioners.

Pioglitazone improved insulin sensitivity and altered cortisol metabolism in PCOS patients.

Zinc pyrithione needs targeted delivery to the scalp for effective dandruff treatment.

Different genes are active in dogs' hair growth and skin, similar to humans, which helps understand dog skin and hair diseases and can relate to human conditions.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

The document concludes that an experimental drug may help wound healing in Epidermolysis Bullosa, links Hydroa vacciniforme to EBV, discusses diagnosing hair loss disorders, finds many children with eczema have allergies, reviews the safety of a skin medication in children, notes side effects of a Duchenne's treatment, and identifies a marker for pediatric mastocytosis.

Oral isotretinoin temporarily improved skin symptoms in a child with IFAP syndrome.

A child with Olmsted syndrome showed mild improvement in hair and skin issues with treatment.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

A woman with CHILD syndrome showed skin abnormalities, and the report suggests CHILD nevus and NEVIL might be the same condition, highlighting the need for diagnosis for genetic advice.

Some skin diseases and their treatments can negatively affect male fertility.

Surgery on a baby with a skin disorder improved eyelid position and eye health.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

The document concludes that the girl's hairlessness is likely inherited from her parents.

New technologies help us better understand how skin microbes affect skin diseases.

Hair changes can indicate systemic diseases or medication effects.

Keratosis pilaris is often linked to genetic mutations and causes skin and hair abnormalities, regardless of those mutations.

Mutant mice help researchers understand hair growth and related genetic factors.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

Androgenic steroids can slow down or stop the growth of certain skin fungi.

High levels of ST14 and TMEFF1 proteins in ovarian cancer are linked to worse patient outcomes and may be a new treatment target.

Mimicking growth factors in a topical solution can prolong hair growth phase and reduce hair loss without side effects.

A woman's nail separation was likely caused by poor blood flow, and a treatment for similar conditions might help.

Looking at skin can help find and treat serious diseases early.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

The TGM3 gene's promoter region is key for skin and hair cell function and may aid gene therapy.

Lack of cystatin M/E causes thin hair and dry skin.