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A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Methylene blue staining effectively reveals detailed nerve structures in rat snouts.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

The newborn's skin blistering is due to a genetic condition called epidermolytic hyperkeratosis.

The woman's forehead lesion was caused by ointment use and resolved with treatment.

GABEB is a less severe skin condition caused by a gene mutation affecting collagen, leading to blisters and other symptoms.

Reflectance confocal microscopy can noninvasively diagnose onychomatricoma by showing unique features different from healthy nails or nail fungus.

Mutations in the KRT16 gene can cause skin and nail disorders.

"20-nail dystrophy" can have multiple causes.

Erosive pustular dermatosis of the scalp is a type of skin inflammation often confused with other conditions, requiring continuous treatment.

The specific skin disease variant p.(Arg2000Trp) in plectin can cause a wide range of symptoms, which should be considered when diagnosing patients.

EPDS is a rare, chronic scalp condition that's hard to treat and needs better awareness for improved outcomes.

A rare scalp infection in a child developed into a kerion with additional skin symptoms.

Hair gels may cause split ends in children.

Podiatrists need more training to detect foot melanoma early.

Most people with alopecia areata have nail changes, which are common but don't greatly affect their quality of life.

Hair and nail cells share similar proteins, indicating a common differentiation pathway.

Trichodaganomania involves biting one's hair and needs combined psychological and medical treatment.

Trichosporon inkin and Trichosporon mucoides can cause white piedra on scalp hair.

Ponatinib can cause a rare skin reaction that resolves with topical treatment and temporary drug discontinuation.

Two sisters with Netherton's syndrome had skin and hair issues, needing special diet and ointments.

Olmsted syndrome is a rare skin disorder causing thickened skin and other symptoms.

A man's pubic hair infection was treated by shaving and using antifungal medications.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

Cathepsin E is crucial for normal skin cell differentiation and development.

The glassy layer of hair follicles has different fibril sizes and arrangements in guinea pigs and young mice.

Exosomes help hair follicle development in cashmere goats.

Pityriasis rubra pilaris is a rare skin disorder with reddish-orange patches and thickened skin, needing better treatment understanding.

A rare skin reaction from cancer treatment was successfully managed with topical treatments and antihistamines.