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A 7-month-old girl with a rare skin disorder died because diagnosis was delayed.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Actinic keratosis can lead to skin cancer, is more common in fair-skinned people, and can be reduced with sunscreen and treated effectively.

Two boys developed a viral skin infection during chemotherapy, which resolved with improved immune function.

The study found unique skin changes in a rare type of alopecia linked to a skin condition called linear morphea.

Laser treatments are the most effective for porokeratotic adnexal ostial nevus.

KID syndrome should be reclassified as an ectodermal dysplasia.

Hair shaft dysplasias are abnormal hair conditions that can be inherited or acquired and may signal other health issues, with limited treatment options available.

iPSCs can help treat genetic skin disorders by creating healthy skin cells from a small biopsy.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

A 7-year-old girl had a non-painful skin growth at her belly button, which was removed and identified as a keratinous cyst.

Symmetrical Acrokeratoderma (SAK) may be a unique skin condition in China, lacking specific treatment and needing long-term monitoring.

A 19-month-old boy with a rare hair disorder showed mild improvement with treatment, but his family chose gentle hair care due to limited success.

The young goat had anaplasmosis and copper deficiency.

Early diagnosis and lifelong zinc supplementation are crucial for treating acrodermatitis enteropathica effectively.

EGFR deficiency in skin causes hair follicle issues and inflammation.

A 10-month-old boy with a rare combination of genetic conditions has severe immune deficiency and treatment challenges.

Punctate follicular porokeratosis is a skin condition with specific features seen in hair follicles.

The treatment for alopecia areata with diphenylcyclopropenone was unsuccessful.

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

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.

TAF can be identified by excessive skin thickening and clogged hair follicles, helping distinguish it from similar skin conditions.

Deleting the CD271 gene in mouse skin cells leads to disorganized skin and increased hair growth, suggesting CD271 is important for skin health.

Alopecia can be a symptom of Neonatal Lupus.

People with Down syndrome are more likely to have alopecia areata and need regular skin check-ups.

A heart transplant patient developed a skin condition called epidermodysplasia verruciformis after taking immune-suppressing drugs.

Familial dyskeratotic comedones are a rare, benign skin disorder that is hard to treat.

A hair growth ointment improved hair length in a family with a genetic hair growth condition.