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Testosterone therapy aims to treat hormone deficiencies and various conditions safely and effectively, but requires careful patient monitoring due to potential side effects.

Self-amplifying RNA could be a better option for protein replacement therapy with lower doses and lasting effects, but delivering it into cells is still challenging.

Reflectance confocal microscopy is a useful, non-invasive tool for diagnosing some skin diseases, with potential for future improvements.

Hair follicles are essential for skin health, aiding in hair growth, wound healing, and immune function.

An 18-year-old girl was diagnosed with a rare hereditary hair loss condition, despite no family history.

Caffeine may help hair growth in hereditary hair loss.

Caffeine in Alpecin shampoo may help prolong hair root activity and reduce hair loss.

The emulgel with specific ingredients was effective for treating hair loss.

A man's chest hair turned white after a shingles infection, possibly due to virus-damaged pigment cells.

The meeting discussed medical findings, including benefits of certain treatments for cancer and heart conditions, and highlighted issues like poor adherence to preventive measures and skill gaps among interns.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

Trichoscopy is useful for diagnosing hair and scalp disorders in people with darker skin.

Some women with common hair loss may develop permanent hair loss.

Micrografts promote hair growth in androgenetic alopecia treatment.

Notch-related genes play a key role in the development and cycling of hair follicles.

Nail loss may be a side effect of the MS drug teriflunomide.

SA linked to mitochondrial issues and oxidative stress, while AGA involves disrupted hair growth genes.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

Screening for iron levels in patients with hair loss may help find a genetic iron overload condition early.

Marie-Unna Hereditary Hypotrichosis is a rare genetic condition causing sparse hair growth, requiring specific recognition for proper care.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

The first Japanese family with Marie Unna hereditary hypotrichosis showed hair condition improvement in a child and highlighted the risk of misdiagnosis.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

Researchers found a gene mutation responsible for a rare hair loss condition.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

Isotretinoin may effectively treat hereditary hypotrichosis simplex, a rare hair loss condition.

A mutation in the SREBF1 gene causes both hereditary mucoepithelial dysplasia and IFAP syndrome, which are related conditions.

A girl with hereditary chorea, likely Huntington's disease, had her condition worsened by lupus.