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New hair regrowth model introduced, imiquimod kills skin cancer cells, T-cadherin loss makes skin cancer more invasive, no strong link between PTCH1 gene and skin cancer after transplant, and male teens more likely to have hereditary hair loss.

The four patients have a unique type of ichthyosis affecting hair follicles.

Systemic mastocytosis may cause a type of hair loss called cicatricial alopecia.

Dermoscopy helps distinguish between scarring and non-scarring hair loss and accurately diagnoses hair and scalp conditions without needing hair plucking.

An 8-year-old girl had nail and hair issues that improved without specific treatment, but fungal nail infection was hard to cure.

Keratin 15 cells from hair follicles help develop and maintain skin tumors in mice.

Trichoscopy is a useful tool for monitoring hair and scalp diseases.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

Alopecia mucinosa is a challenging condition with unclear diagnosis and treatment.

Tinea capitis needs systemic treatment to avoid severe outcomes.

Most cases of Temporal Triangular Alopecia are found in early childhood and may be related to genetic conditions.

The document describes previously unreported unique skin changes in a rare genetic disorder called Hereditary mucoepithelial dysplasia.

Basal cell carcinoma may originate from vellus hair cysts.

A man's unusual scalp folds caused by a skin condition were treated with surgery and remained unchanged two years later.

Onychomatricoma is a unique nail tumor that mimics the entire nail unit and is not related to other hair-related tumors.

Some patients with a type of skin lymphoma can experience a rare, non-scarring hair loss that looks like another hair loss condition but has distinct features.

An 8-year-old boy with hair-pulling disorder had a bald patch that was confirmed not to be a fungal infection and was treated with therapy.

LHTric-1 is a specific antibody useful for studying hair and nail formation.

Mutations in the hairless gene cause hair loss and skin cysts in rhesus macaques.

A woman had a unique skin growth with hair follicle, oil glands, fat cells, spindle cells, and nerve fibers.

Special scalp and hair examination techniques can identify hair problems.

Specific brain and bone imaging findings can help diagnose Trichothiodystrophy.

Trichoscopy is a useful non-invasive method for diagnosing different hair loss conditions.

RET mutation is important in familial medullary thyroid carcinoma, and BRAF mutation in papillary thyroid carcinoma is linked to more aggressive cancer and higher death rates.

A 3-year-old boy was diagnosed with a rare, non-scarring hair loss condition called temporal triangular alopecia.

A 23-year-old Syrian woman has two rare hair disorders, and avoiding hair treatments plus using vitamins and minoxidil may help.

Children with alopecia areata have different trichoscopic features than adults, including more empty follicular openings and pigtail hairs.

Avoiding damage and using specific shampoo and supplements improved the hair condition.

External factors like certain shampoos, bacterial infections, and parasites might cause hair defects similar to genetic conditions.