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A new gene variant causes glucocorticoid resistance in a mother and son.

Finasteride may effectively treat hair loss in Klinefelter Syndrome patients.

Leptin affects skin and hair health and may worsen some skin conditions, but more research is needed to understand its full impact.

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

A man with both Klinefelter syndrome and primary hyperparathyroidism showed a rare combination of symptoms and genetic patterns.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Imatinib mesylate can cause skin lightening, especially in Chinese patients, due to its effect on pigment production.

Finasteride shows promise for treating hair loss and excessive hair growth, but more research is needed to confirm its effectiveness and safety.

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

Recognizing oral symptoms can help diagnose and treat blood and nutritional diseases early.

Advanced imaging techniques are crucial for accurately diagnosing Monilethrix, a rare hair disorder.

Vimentin is involved in regulating the hair growth cycle in Inner Mongolian Cashmere goats.

Early diagnosis and genetic evaluation of ADULT syndrome are crucial to reduce stress and medical costs.

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

Despite progress in treatment, the exact cause of Alopecia areata is still unknown.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

A three-year-old girl has hair loss despite treatment with selenium sulfide shampoo and anti-fungal medication.

The transgene likely activated an oncogene or interrupted a tumor suppressor gene, causing melanoma in mice.

Intralesional triamcinolone is the most effective treatment for hair regrowth in alopecia areata patients.

Kennedy's disease leads to muscle weakness and sensory issues, has no cure but manageable symptoms, and future treatments look promising.

Interferon, especially alfa interferon, is an effective treatment for cutaneous T-cell lymphoma with manageable side effects.

Found different long non-coding RNAs in balding Chinese men, which may help create new treatments.

Sex hormones may affect COVID-19 severity, with men often faring worse, and targeting related pathways could offer treatment options.

ALA-PDT is effective and safe for chronic X-ray dermatitis, providing complete or partial remission.

Non-coding RNAs could help detect and treat radiation damage.

Sex hormones may affect COVID-19 severity, with estrogen possibly reducing risk and testosterone potentially increasing it.

Women with myotonic dystrophy might get diseases related to male hormones because their body tissues are extra sensitive to these hormones.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

FOXN1 mutations cause severe immunodeficiency, hair loss, nail issues, and thymus defects.