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Scientists found a new type of skin cell that could help with skin repair and these cells work better with a certain protein.

New LPP subtype affects vellus hairs, mimics AGA, and needs biopsy for diagnosis.

Mutations in the hairless gene cause a rare form of permanent hair loss.

Dermoscopy is useful for diagnosing Atrichia with Papular Lesions in children without needing a biopsy.

Scarring alopecia involves increased immune cells and specific gene changes near damaged hair follicles.

Lupus panniculitis of the scalp causes linear hair loss and needs ongoing treatment to prevent recurrence and lupus.

Trichoscopy helps tell apart Frontal Fibrosing Alopecia and Lichen planopilaris by showing different hair and scalp features.

Four new cases confirmed the unique features of follicular porokeratosis.

The method shows how hair lipids form specific patterns and their roles in hair structure.

Platelet-rich plasma might be a new way to treat lichen planopilaris.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

Steroid injections are more effective than platelet rich plasma for treating patchy hair loss.

Postmenopausal frontal fibrosing alopecia may be a unique condition linked to postmenopausal changes.

Acitretin helped improve hand mobility and skin condition in a patient.

Hair evaluation is crucial for early diagnosis and management of ARCI, as hair loss often indicates severity.

New understanding of the causes of primary cicatricial alopecia has led to better diagnosis and potential new treatments.

Two cases of a rare skin condition were successfully treated with laser therapy, offering a non-surgical treatment option.

Alopecia areata can look like frontal fibrosing alopecia, making diagnosis hard.

The woman was diagnosed with lichen planopilaris and can be treated with corticosteroids.

FFA is more common in postmenopausal women, can affect younger women, and may stabilize over time.

Stem and progenitor cells in the eye have different division rates and locations, affecting how they respond to injury.

PAON shows skin patterns due to genetic mosaicism.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

RCM and dermoscopy help identify different types of hair loss in children.

The gene LRRC15 is more active in balding areas of the scalp compared to non-balding areas.

New hair loss subtype found, mimics common baldness.

A patient with a thick scalp and hair loss was correctly diagnosed with alopecia areata and a thick scalp fat layer, not lipedematous alopecia, and regrew hair after treatment.

GLPLS and LPP are variants of lichen planus.