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The patient has frontal fibrosing alopecia (FFA).

A 46-year-old man was diagnosed with frontal fibrosing alopecia, a condition usually seen in postmenopausal women.

The document concludes that post-menopausal frontal fibrosing alopecia is a poorly understood condition that does not respond well to common treatments.

A woman's nail separation was likely caused by poor blood flow, and a treatment for similar conditions might help.

Frontal Fibrosing Alopecia involves disrupted cholesterol pathways, fibrosis, and increased mast cells.

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

Fibroblast changes in systemic sclerosis may help understand disease severity and treatment.

A woman with Parry-Romberg syndrome developed new curly hair on one side of her scalp, a condition not previously linked to the syndrome.

A young boy with a rare skin and nail condition improved significantly with simple topical treatments.

Frontal fibrosing alopecia is a challenging hair loss condition with no known cause or definitive treatment.

Frontal fibrosing alopecia is a scarring hair loss condition mainly affecting postmenopausal women, with unclear causes.

Familial frontal fibrosing alopecia is rare, mostly affects women, and often occurs between sisters or mother-daughter pairs.

Frontal fibrosing alopecia may run in families.

Frontal Fibrosing Alopecia is a slowly progressing hair loss condition, likely underdiagnosed, with ineffective treatments, needing more research to understand it fully.

Genetic testing can help diagnose skin conditions but needs more research for full effectiveness.

Avoiding friction and using topical treatments can significantly improve rough skin caused by repeated rubbing.

Fibrosing alopecia in a pattern distribution is a new type of scarring hair loss that resembles common baldness and an autoimmune skin disease.

Children with Parry Romberg Syndrome had successful facial fat-grafting surgeries after disease stabilization with no complications.

Tofacitinib can cause skin eruptions similar to palmoplantar pustulosis.

These hair loss conditions might be part of a spectrum, not separate issues.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

Frontal fibrosing alopecia mainly affects women over 50, causing hair loss and specific skin changes.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

FAPD is a possible diagnosis for hair loss in patients of color and requires multiple evaluations for accurate diagnosis.

Frontal fibrosing alopecia can cause sudden hair loss on limbs, similar to scalp hair loss.

Fibrosing alopecia can be stabilized or improved with anti-inflammatory treatments and hair growth agents.

Follicular porokeratosis may be linked to diabetes and can lead to hair loss.

Pityriasis rubra pilaris is a rare skin disorder with reddish-orange patches and thickened skin, needing better treatment understanding.

Vismodegib is effective for basal cell carcinoma but has severe side effects.