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Certain drugs can change hair color, either lightening or darkening it.

A man in his 30s had patchy hair loss on his leg due to primary follicular mucinosis.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

A woman with breast cancer developed a rare condition causing excessive fine hair growth on her face and body.

Women with PCOS have distinct retinal changes compared to healthy women.

Combining surgery and photodynamic therapy effectively treated a rare scalp condition when other treatments failed.

Pseudopelade of Brocq is a unique hair loss condition, but its cause and development are still not fully understood.

Minoxidil use was linked to a rare eye condition that improved after stopping the treatment.

Hyperaesthetic leucotrichia in horses causes painful, recurring skin lesions and hair color changes, especially in Arabian and American paint horses.

A 5-year-old boy's skin condition improved with systemic valganciclovir after a cardiac transplant and immunosuppressive therapy.

Graves' disease often causes skin issues, especially hyperpigmentation, which may be linked to treatments.

Folliculitis Decalvans and Frontal Fibrosing Alopecia can coexist in people with darker skin, showing features of both conditions.

Significant progress was made in understanding PXE, but effective treatments are still needed.

Verteporfin reduces growth and stem cell traits in rat hair follicle cells by blocking the Hippo pathway.

A specific group of early-stage melanocytes is reduced in vitiligo-affected skin, which may explain treatment resistance.

A man with a skin nodule was diagnosed with a rare skin condition called cutaneous focal mucinosis, which can be confused with other skin cancers.

Pilomatricomas should be considered to avoid misdiagnosis in children with unusual skin tumors.

Combining hair follicle transplantation and a 308 nm excimer laser effectively treats perioral vitiligo without unwanted hair growth.

A Japanese patient with a rare genetic disorder had a less severe case than others, suggesting other factors may affect symptoms.

Buschke-Ollendorff syndrome is a rare genetic disorder causing skin and bone changes, with some cases also showing ADHD or developmental delays.

Dermoscopy is useful for diagnosing lichen planopilaris and certain features may relate to disease duration, age, and gender.

Combining laser with PRP is more effective for vitiligo than PRP alone.

Mutations in the KRT85 gene cause hair and nail problems.

A baby with KID syndrome died from infections and organ failure at 18 months old.

The document concludes that a protein involved in hair growth may link to baldness and that more research is needed on its role in hair loss and skin cancer treatments.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Blocking the JAK/STAT pathway may help reduce skin sensitivity in Xeroderma pigmentosum.

Purpura fulminans can signal underlying autoimmune disorders, not just infections.

Surgical removal of abnormal fat pads fixed the woman's eyelid issue caused by likely silicone injections.