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A new mutation in the Hairless gene causes hair loss in two Pakistani families.

Scalp melanoma is more common and easier to diagnose early in people with androgenetic alopecia due to sun damage.

Acitretin significantly reduced inflammatory attacks in a woman with Naevus Comedonicus Syndrome but caused side effects.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

IPL treatment can significantly reduce hair in faun tail but may need local anesthesia.

New insights in skin conditions show a complex link between certain moles and melanoma, improved hair loss treatments, and the need to identify different types of lupus.

A kidney transplant patient on cyclosporin experienced unexpected severe hair loss, which improved with treatment adjustments.

The document concludes that unruly hair can be congenital or acquired, often lacks specific treatments, and can be managed with oils and short hairstyles.

Photodynamic therapy was effective in treating multiple scalp basal cell carcinomas with minimal side effects and good cosmetic results.

A 10-year-old boy had the earliest reported case of hair that became progressively kinkier but eventually returned to normal on its own.

A clinically suspected melanoma appeared benign under the microscope but was confirmed by specific tests and a rare mutation.

Botulinum toxin has potential for treating various skin conditions and improving wound healing.

A 17-year-old developed woolly hair nevus in adolescence, which is unusual, and over time the hair darkened and straightened slightly, but microscopic changes persisted.

Asian immigrant mothers in Leicestershire need better obstetric care to reduce higher perinatal mortality risks.

SACUMAN, a rare condition causing hair loss without clear signs, is often misdiagnosed and needs scalp biopsies for accurate detection.

Topical vitamin D is useful for some skin conditions but not effective for others, and more research is needed.

Trichoscopy is reliable for diagnosing Temporal Triangular Alopecia and can prevent unnecessary biopsies and wrong treatments.

People with Lichen planopilaris are more likely to have certain autoimmune and endocrine disorders but less likely to have conditions like allergies and diabetes.

Yellow and orange colors are important for diagnosing certain skin conditions.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.

Children with short anagen syndrome usually see their hair condition improve as they get older.

A baby had a rare condition with abnormal blood vessels in the brain and unusual skin and hair growth, possibly a new syndrome.

The document suggests a rare skin condition might be caused by a genetic phenomenon.

The boy with woolly hair nevus had thinner hair and abnormal hair follicles, which improved with treatment but worsened when treatment stopped.

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

A girl with a rare syndrome had successful hair loss treatment with no relapse after 4 years.

A rare combination of halo nevi, nonsegmental vitiligo, and early gray hair can occur together.

Antigens from skin cells may cause hair loss in perinevoid alopecia.

The document provides a comprehensive index of medical and surgical topics, including hair removal, hair restoration, and various treatments for injuries and conditions.

Hair loss and excessive growth treated with various options, including new laser technology.