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Scientists used stem cells to create a model of the skin disease Epidermolysis Bullosa simplex, which helped them understand its molecular mechanisms and could aid in finding treatments.

Monkeys with more anxious or inhibited temperaments tend to have less hair loss.

Reductive stress messes up collagen balance and alters cell signaling in human skin cells, which could help treat certain skin diseases.

Genetic defects in the Wnt/PCP pathway may cause congenital yellow nail syndrome.

FAKΔe4 helps cells sense and respond to different stiffness levels in their environment.

The Brigham Eyebrow Tool for Alopecia is a simple and reliable way to measure eyebrow hair loss.

A 6-year-old boy's leg hair loss was due to friction from sitting cross-legged, and it usually resolves on its own.

Thiamin deficiency might cause hair loss and mental health issues.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

The pseudo 'fringe sign' can also appear in frontal fibrosing alopecia, not just in traction alopecia, showing that this condition may be more common than thought.

Hoxc13 gene is essential for hair, nail, and papilla development.

Removing both Atr and Trp53 genes in adult mice causes severe tissue damage and death due to DNA damage.

Aluminum phosphide poisoning can cause horizontal nail grooves and hair loss.

Uncombable hair syndrome causes dry, frizzy hair that can't be combed flat, seen in a young child.

The newborn was diagnosed with a rare skin disorder causing blisters, which requires careful wound care and family support.

The study found no link between anxiety, vitamin B12, folate, TSH, ferritin, zinc levels, and trichodynia in telogen alopecia patients.

Four children had unmanageable pale blond hair due to uncombable-hair syndrome.

Chemical stressors damage hair structure but the skin's outer layer protects living cells.

Frontal fibrosing alopecia can mimic traction alopecia but has distinct features like facial papules and eyebrow thinning.

Low-sulfur hair syndrome can cause UVB sensitivity and testicular failure.

Chemotherapy caused a woman's permanent hair loss and early menopause.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Selenium and zinc deficiency in sheep leads to thyroid and skin problems.

A gene mutation in mice causes hair loss, weak bones, and protein buildup, showing how protein processing issues can lead to diseases.

Stretched hair has a similar structure to natural silk, showing hair's elasticity involves reversible changes within its molecules.

Keratin is crucial for skin barrier formation and affects mitochondrial function.