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Localized dystrophic epidermolysis bullosa (DEB) can lead to scarring alopecia, highlighting the need to recognize and address this complication.

Mutations in the KLHL24 gene cause skin blistering in epidermolysis bullosa simplex.

An 8-year-old girl developed a rare skin condition in a linear pattern on one side of her body after a lung infection, which improved with treatment.

A rare skin condition in children can look like other diseases.

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

Chronic scalp lesions with crusts and pus that heal with strong topical steroids suggest Erosive Pustular Dermatosis, confirmed by biopsy showing specific immune cells.

Bardet-Biedl syndrome may include under-recognized skin problems related to its metabolic disturbances.

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

Non-itchy rashes can indicate serious diseases like lupus.

Follicular atopic dermatitis in dark skin can look different, making diagnosis harder.