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Papular mucinosis can cause eyebrow hair loss, but treatment can lead to regrowth.

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

Pseudofolliculitis barbae is a chronic skin condition affecting mainly African American and Hispanic individuals, caused by shaving tightly curled hair, and managed by prevention and treatment but not curable.

A man with a weakened immune system was diagnosed with a rare skin condition called trichodysplasia spinulosa using skin examination techniques.

Frontal fibrosing alopecia and ulerythema ophryogenes may be related and can evolve from one to the other.

Two unusual cases showed that Lichen Planopilaris can look like other skin conditions and need early treatment to protect hair.

A woman's ovarian fibroma caused high testosterone levels, which normalized after surgery.

A 69-year-old woman has a fast-growing hand lesion that didn't improve with salicylic acid.

Congenital triangular alopecia is a harmless, non-spreading hair loss condition often seen in young children.

Benign skin adnexal tumors are more common than malignant ones, with trichoepithelioma and chondroid syringoma being the most frequent types.

Oral lichen planus can appear before lichen planopilaris.

Folliculotropic Mycosis Fungoides requires stage-based treatment, with early stages using skin therapies and advanced stages needing aggressive treatments.

Plica polonica is a rare condition where hair becomes irreversibly tangled, and the treatment is to cut the matted hair.

Plucked hair can help diagnose pemphigus vulgaris early.

Women with Frontal Fibrosing Alopecia have more wrinkles near their ears than similar aged women without the condition.

OCT can non-invasively diagnose follicular keratosis and other hair follicle disorders.

Frontal Fibrosing Alopecia may be a complex condition linked to hormonal changes in women, not just a form of Lichen Planopilaris.

A rare foot cyst was successfully diagnosed and removed without cancer.

A woman with a rare form of multiple myeloma had a headache and a skull mass, which led to her diagnosis after tests and a biopsy.

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

PRAME helps distinguish between benign and malignant skin cells in most cases.

Researchers found a new early sign of Frontal Fibrosing Alopecia that could help avoid misdiagnosis.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

A 70-year-old woman with a rare skin condition improved after treatment with topical steroids and acitretin.

Erythematous papulopustular eruptions in cancer patients using EGFR inhibitors show specific skin changes that vary with severity and treatment type.

Surgery may help infants with sagittal craniosynostosis develop more typical language processing.

Onyx® embolization effectively treats facial arteriovenous malformations with minimal complications.

Combining treatments significantly reduces dark circles and wrinkles better than nanofat alone.

Postoperative folliculitis after hair transplants is a minor issue that doesn't relate to patient details or how much hair is transplanted.

Sudden, unusual hair loss may indicate serious underlying health issues.