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Two people had unusual ring-shaped hair loss due to an autoimmune disorder.

Onycholemmal horn is a rare nail tumor in elderly women, treated by surgical removal.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

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

Spironolactone may help enlarge a small breast linked to Becker's nevus.

Nestin-expressing hair follicle cells may be useful for nerve repair and regeneration.

A 16-year-old boy had pernicious anemia, autoimmune hemolytic anemia, and later developed alopecia areata.

The neck mass was a rare benign "wattle," surgically removed for diagnosis and appearance.

HLA can be linked to autoimmune hepatitis.

New microneedles may improve vitiligo treatment.

Eruptive vellus hair cysts are rare and often misdiagnosed, requiring biopsy for accurate diagnosis.

Two newborns with rare skin infections were successfully treated with antifungal cream.

A woman's shingles infection triggered her first episode of a rare neurological disorder and blood vessel inflammation.

A 32-year-old woman's hair loss was linked to skin nodules and severe headaches.

Fungal infections should be considered in scalp swelling to avoid misdiagnosis.

Recognizing perinevoid alopecia and concentric regrowth is important for diagnosing and treating alopecia areata.

Spotted lunula may help identify alopecia areata.

Certain gene variations may increase the risk of alopecia, and platelet-rich plasma treatment can improve hair density in those with hair loss; a rare case of facial Becker's nevus was linked to uneven beard growth.

Diode laser treatment effectively clears acne keloidalis nuchae.

Homeopathy improved Acne Keloidalis Nuchae in a 14-year-old.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

Kerion is a rare but serious scalp infection that needs proper treatment.

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

A person with a new mutation in the SCN1A gene developed brain inflammation after COVID-19.

Better diagnostic and treatment strategies are needed for acne keloidalis nuchae, especially in high-risk groups.

Macular alopecia is a distinct, non-scarring hair loss pattern that mostly affects young Hispanic/Latinx females and often resolves on its own.

Schimmelpenning Syndrome requires careful evaluation and tailored treatment for skin, eye, and developmental issues.

A condition with certain scalp changes may come before acne keloidalis nuchae and other similar hair loss disorders.

Current treatments for neutrophilic alopecias in children are limited and often ineffective, especially for males and those of Afro-Caribbean descent.

An adult had a rare scalp infection in the forehead area, treated successfully with itraconazole.