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Female donor to male recipient sex mismatch and positive ACA-IgG are key risk factors for vitiligo and alopecia areata in chronic GvHD patients.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

Genetic discoveries are leading to new treatments for alopecia areata.

A rare scalp condition can occur due to leukemia affecting the skin.

A family had a genetic condition causing hair loss on the scalp, passed down through four generations.

Alopecia areata does not affect areas with psoriasis plaques.

A 10-year-old boy recovered from a scalp infection caused by a fungus after treatment with itraconazole.

Majocchi's granuloma can occur in kidney transplant patients on tacrolimus and can be treated with antifungal medication.

Traumatic anserine folliculosis is a harmless skin condition in young males that needs correct diagnosis to avoid unnecessary treatments.

Alopecia areata is a hair loss condition that often starts before age 30 and can affect various body parts, with unpredictable hair regrowth chances.

The MTHFR C677T mutation may increase the risk of alopecia areata in the Turkish population.

Alopecia and acne in women are complex conditions needing coordinated care and personalized treatment.

Acne treatment with isotretinoin increases the presence of p53, a protein, in skin and oil glands, which may help reduce acne severity.

Two siblings were the first reported cases of inheriting both eye coloboma and loose anagen syndrome together.

The role of γδT-cells in causing alopecia areata remains unclear.

Alopecia areata is an autoimmune disease with genetic links, treatable with certain medications, and can affect mental health.

A woman on immunosuppressants developed two rare scalp conditions, which improved with specific treatments.

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Increasing zinc intake improved skin and hair symptoms in a rare genetic disorder.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

Symmetrical Acrokeratoderma (SAK) may be a unique skin condition in China, lacking specific treatment and needing long-term monitoring.

The boy's symptoms suggest a possible new medical condition.

The angora mouse mutation causes long hair and hair defects due to a gene deletion.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

A mother and son both had ulcerative colitis and alopecia, suggesting a genetic link in autoimmune disorders and successful treatment with cyclosporine.

A girl with symptoms like an autoimmune disorder actually had HIV and a fungal infection, which was hard to diagnose and treat, leading to her death.