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A baby boy had two types of temporary hair loss at birth, which might be two forms of newborn hair loss combined.

Bone mineral and minocycline boost bone cell growth, aiding healing.

A new method allows detailed, continuous imaging of crustacean leg regeneration without harming the cells.

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

The Sacred Heart Bilobed Flap is a surgical method for repairing small scalp defects with local flaps, relying on scalp elasticity and hair regrowth to hide any imperfections.

Systemic steroids effectively treated severe nail issues in a card illusionist with alopecia areata.

CIP/KIP proteins help stop cell division and support hair growth.

The African spiny mouse can fully regenerate its muscle without scarring, unlike the common house mouse.

A 14-year-old girl with no menstrual period was diagnosed with Swyer Syndrome and treated for a related cancer risk.

A new method allows detailed tracking of cell regeneration in crustacean legs.

A supernumerary nipple was correctly identified using dermoscopy, avoiding misdiagnosis.

Hair matrix cysts are rare skin nodules with unique features, often needing surgical removal.

Spiny mice can regenerate tissues instead of forming scars.

Understanding how baby skin heals without scars could help develop treatments for adults to heal wounds without leaving scars.

Frontal fibrosing alopecia and ulerythema ophryogenes may be related and can evolve from one to the other.

A cross-bred lamb with severe skin and movement issues had ichthyosis fetalis but normal vitamin A levels.

Piperonylic acid speeds up wound healing by reducing inflammation and boosting collagen.

Gene and cell therapies are being developed to treat rare skin conditions like epidermolysis bullosa and ichthyosis.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

Half-siblings with a rare skin condition improved with treatment for a fungal infection, but hair loss remained.

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

Both tissue expansion and serial excision are effective for scar revision in the head and neck area.

Understanding cell transitions can lead to better wound healing treatments.

Pili annulati is caused by a protein metabolism disorder affecting hair structure.

Early recognition and treatment of EPDS are crucial to prevent permanent hair loss.

A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.