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Small proline-rich proteins and trichohyalin help make epithelial tissues tougher and more flexible.

The woman was diagnosed with lichen sclerosus, a rare skin condition, after initial misdiagnosis and ineffective treatments.

A specific gene mutation causes sparse, brittle hair in a family.

Taiwan reported its first case of a rare scalp condition with no clear cause or treatment.

Hairless USP mice have enlarged skin cysts as they age.

A Holstein calf in Iran with a severe genetic skin disorder was euthanized due to incurable symptoms.

People with hidradenitis suppurativa often have lower vitamin D levels, weaker hip bones, and altered bone metabolism markers.

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

The study found increased skin pigmentation and variable melanocyte density in a patient with Addison's disease.

Isolated patchy heterochromia with pili annulati can occur without other health issues.

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

Hereditary elliptocytosis causes elongated red blood cells and can lead to mild or no symptoms.

If someone has scaly skin, muscle stiffness, and intellectual disability, doctors should consider Sjogren-Larsson Syndrome, but other conditions if more symptoms are present.

The patient's hair has unique structural differences with alternating bright and dark bands.

Er:YAG laser therapy effectively treats Hailey-Hailey disease, leading to long-term remission and improved quality of life.

Treatment with moisturizers improved the skin condition of a girl with a rare genetic skin disorder.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

Antifungal treatment can improve severe skin infections with cutaneous horns.

The patient has a leg condition caused by vein issues, needing lifestyle changes and leg care.

A man with both skin lesions and lung cancer improved quickly with chemotherapy, suggesting the skin condition might be a reaction to immune system injury.

Rothmund-Thomson syndrome causes skin changes, hair loss, and slightly high lysine and cystine in urine.

Careful light microscopy is crucial for detecting mild cases of pili annulati, which weakens hair and varies widely in expression.

pCLCA2 protein may help maintain skin structure and function.

A rare skin condition usually on the face was found on a man's heel.

Trichohyalin, a hair follicle protein, has a part with repeating patterns of 23 amino acids.

The man has a genetic skin condition called pachyonychia congenita.

Infrared light, alone or with hyaluronic acid, effectively treats skin laxity with minimal side effects.

Hyaluronic acid injections can cause serious artery blockages, so practitioners must be careful.