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

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

Lichen planopilaris causes permanent hair loss and scarring due to damage to hair follicles and can be mistaken for other hair loss conditions.

A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.

Narrowband UVB therapy significantly improved a child's rare skin condition.

HPV8 causes hair follicle stem cells to grow, leading to skin lesions.

CD19-CAR T cell therapy may help regenerate skin in systemic sclerosis.

Trichilemmal keratinization is a unique process in hair follicles where the outer root sheath turns into keratin without a specific layer.

New mutations in the DSG4 gene cause a rare hair condition.

Graham-Little Piccardi Lassueur Syndrome is a rare skin condition with specific hair loss and skin symptoms.

Lichen Planopilaris causes irreversible hair loss due to immune attacks on hair stem cells, but modulating PPAR-γ might help treat it.

Netherton's syndrome may have a familial link and doesn't always include atopy.

A man in Japan got better from a scalp fungal infection using terbinafine.

A unique hair tumor with a rippled pattern was identified, showing incomplete differentiation and unusual cell arrangements.

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

A boy's scalp rash and baldness were cured using oral medication and medicated shampoo.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

Lichen planopilaris mostly affects women with fair skin and can look different on each person, needing early treatment to prevent hair loss.

Capsaicin cream quickly relieved itching in two patients with brachioradial pruritus.

A skin condition called pyodermatitis vegetans was found in a patient with multiple myeloma for the first time.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

A specific mutation in the TRPV3 gene causes hair follicle cells to develop improperly, leading to hair loss.

Lichen Planopilaris and Frontal Fibrosing Alopecia may help us understand hair follicle stem cell disorders and suggest new treatments.

Dermoscopic and histopathological features combined can help diagnose Pityriasis versicolor.

Dermoscopy can help diagnose secondary syphilis by distinguishing it from other skin issues.

A 12-year-old girl was misdiagnosed with alopecia areata but actually had a nevus sebaceus with a genetic mutation.