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A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

A woman with chronic hepatitis C had a rare skin condition linked to her illness.

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

Clouston's syndrome is a rare disorder affecting nails, hair, teeth, and skin, caused by a gene mutation, and currently has no treatment, only supportive care.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

Ingrown hairs are a common feature in scarring alopecias due to follicular damage.

Eyebrow reconstruction using hair follicle grafts was successful in a man with a benign hereditary disorder affecting his eyebrows.

Hair and nail disorders can cause changes in scalp pigmentation, especially with sun exposure and alopecia.

A woman with dermatomyositis showed rare skin symptoms, was treated successfully, and her case suggests checking for cancer in similar patients.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

A boy with a rare birthmark called verrucous hemangioma needed careful timing for surgery due to its size and depth.

Early diagnosis of Keratosis pilaris atrophicans faciei can lead to better, personalized treatments.

A patient with a rare hair condition and skin disorder showed hair improvement after treatment.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

A rare genetic disease caused severe, worsening hair loss from early childhood with poor treatment results.

Keratin2-6g is crucial for hair follicle development, with mutations causing cell degeneration and vacuolation.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

The conclusion is that the variation in hair thinness in patients is mostly due to the amount of underdeveloped hairs, and treatments that thicken fine hairs might work for those with mild to severe conditions.

Removing ingrown hairs can significantly improve persistent kerion in children.

Trichodysplasia spinulosa can occur after a heart transplant due to immunosuppressive drugs.

A 4-year-old girl has a rare condition causing hairlessness and skin bumps, but normal teeth and sweating.

The man had pretibial myxedema and hyperthyroidism, causing skin changes and thyroid issues.

A new side effect of aromatic retinoid treatment is soft nails.

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

Nevoid basal cell carcinomas start in the skin's top layer and hair follicles.

Overexpression of COX-2 in mice skin causes abnormal skin and hair development.

The patient has a rare skin condition that shows features of two known disorders.

Early biopsy is crucial for diagnosing rare skin sarcoidosis, improving treatment.