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Japanese cases of fibrosing alopecia show a unique age and hair loss pattern, possibly due to racial differences.

Rothmund-Thomson syndrome type 2 can cause chronic, poorly healing wounds.

Diphencyprone therapy for hair loss can cause vitiligo.

Excessive sun protection might contribute to frontal fibrosing alopecia.

A girl with a rare skin condition improved after one month of treatment with acitretin.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

A rare genetic deletion in the KRT1 gene causes unique skin symptoms in a family.

Triple H syndrome exists and can vary in symptoms.

Dermoscopic and histopathological features combined can help diagnose Pityriasis versicolor.

A new gene variant in a girl with Coffin-Lowry Syndrome may link the condition to early puberty.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

Two siblings with a genetic mutation had a form of rickets that doesn't respond to vitamin D.

Certain genes may be linked to autoimmune conditions in people with alopecia areata.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.

The patient likely has Chrousos syndrome, a rare condition causing insensitivity to glucocorticoids, requiring high-dose dexamethasone treatment.

Hashimoto thyroiditis can unexpectedly change into Graves’ disease, so early diagnosis and treatment are important.

A man with Cronkhite-Canada syndrome had all 20 nails detach but improved with treatment.

A specific gene mutation causes varying hair loss severity in a Pakistani family.

A woman with lupus developed a rare skin condition, which improved with increased medication.

Purpura fulminans can signal underlying autoimmune disorders, not just infections.

Intralesional cidofovir may be a viable alternative treatment for SCC.

Rituximab may be an effective treatment for Cronkhite-Canada syndrome with kidney disease.

Cronkhite-Canada syndrome is rare, with high mortality and cancer risk, needing more research for treatment guidelines.

Certain CD8+ T cells attack hair follicles in alopecia areata, suggesting they could be targeted for treatment.

A specific gene mutation causes sparse, brittle hair in a family.

A specific gene variant may increase the risk of developing Alopecia Areata.

Kainar syndrome symptoms may be linked to nuclear test exposure effects.

DM and AA may share a common cause.