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Young women with nonclassic congenital adrenal hyperplasia may experience worse sexual function and mild depression compared to healthy women.

Chronological age affects the mouse auditory cortex more than hearing loss, and the brain may be less sensitive to mitochondrial dysfunction.

Familial dyskeratotic comedones are a rare, inherited skin condition that is hard to treat but may improve slightly with topical retinoids and urea cream.

Male cells need DHT to respond to testosterone, while female cells do not.

Unique fat cells near fibrotic areas contribute to systemic sclerosis progression.

3D cell-derived matrices improve tissue regeneration and disease modeling.

Amelanotic melanocytes from hair follicles are immature and likely don't transfer melanosomes to keratinocytes.

Malnutrition causes skin changes due to nutrient deficiencies.

Mutations in the DSG4 gene cause a severe form of brittle hair and skin issues.

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

Researchers created a new mouse model for studying scleroderma.

Carbohydrates are crucial for skin development and may help understand skin conditions.

DNA methylation changes in Tan sheep affect growth and fur traits.

A patient with Rothmund-Thomson syndrome showed skin changes, hair loss, and dental defects but no cataracts or skeletal issues.

A 15-year-old girl with rare reproductive disorders received hormone therapy to develop secondary sexual traits, but infertility persisted.

Hair loss is caused by the breakdown of a protein called COL17A1 in hair follicle stem cells.

Immature hypertrophic scars on the head and neck have more inflammation and TGF-β, affecting treatment choices.

A litter of cats had a hair condition similar to a mouse mutation, leading to hair loss and abnormal hair and skin.

Apoptosis, not oxidative stress, is linked to aging in mice with mtDNA mutations.

Special proteins are important for skin balance, healing, and aging, and affect skin stem cells.

Aging affects the cells around hair follicles, which may influence female pattern hair loss and treatment options.

EAAT4 decreases with age, harming skin function and calcium balance.

Mutations in the DSG4 gene cause specific hair and scalp issues.

The newborn's skin condition improved over time, leaving only lighter skin patches.

Dsg1 is essential for maintaining a healthy skin barrier in mice.

Metabolic signals and cell shape influence how cells develop and change.

The Korean study found that twenty-nail dystrophy mainly affects adults, more often women, and has five distinct types with different clinical progressions.

Children with severe ichthyosis and growth failure rarely have nutritional deficiencies or gastrointestinal issues, but may experience chronic dehydration.

Monilethrix causes brittle hair and hair loss, and it runs in families.