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

Keratins 8 and 14 can help identify and diagnose benign skin tumors.

Uncombable hair is inherited dominantly with complete penetrance.

A woman with a long-term skin condition developed a serious skin cancer that led to her death.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

Hair follicles in nonsegmental vitiligo are better protected from immune attacks than in alopecia areata.

Alopecia areata symptoms may improve after treating Helicobacter pylori infection.

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

The document concludes that the immune-inhibitory environment of the hair follicle may prevent melanoma development.

Naevoid bundle hair is an unusual hair growth pattern where multiple hairs fuse together.

Porocarcinoma generally has low rates of recurrence, spread to lymph nodes, and death.

Permanent hair loss after a stem cell transplant can be a sign of chronic immune system attack on the scalp.

CK 19 expression is higher in more severe skin cancers.

Two women were diagnosed with a rare melanoma that looked like hair loss but was actually a type of skin cancer.

A woman's male-pattern facial hair growth was caused by a rare malignant ovarian tumor that was difficult to diagnose and treat.

SLHA can be hard to diagnose and needs teamwork between specialists.

Most U.S. keratinocyte carcinoma patients are older white males living in urban areas.

Hair loss is a rare but recognized symptom of pemphigus vulgaris, with patients usually regrowing hair after treatment.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

Bullous pemphigoid can look like erythema multiforme, so awareness is needed for proper treatment.

Congenital atrichia with papular lesions causes permanent hair loss and skin bumps due to a gene mutation.

Porokeratotic eccrine and hair follicle nevus is a very rare skin disorder possibly caused by a GJB2 gene mutation.

Mutations in the LIPH gene cause woolly hair in a child.

Basal cell carcinoma may start from parts of tiny hair follicles.

Dysplastic nevi have unique gene expressions, making them distinct from common melanocytic nevi.

Hepatitis B vaccination can trigger HSP, and vitamin D correction and tonsillectomy can effectively manage it.