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Women with non-classical congenital adrenal hyperplasia have higher levels of certain steroids, which can be reduced by treatment.

Older age and prostatic hyperplasia in males increase the risk of hemorrhagic cystitis after stem cell transplantation.

Gamma/delta T cells help defend skin against heavy metals.

Dual TCR Treg cells are common in mouse tissues and vary by location.

Stem cells in the eye have different roles and behaviors, helping maintain and repair the eye's surface.

Many people diagnosed with androgenic alopecia might actually have hidden scarring or inflammation.

PRO-C22 can help diagnose and monitor the severity of hidradenitis suppurativa.

HS needs personalized treatment plans and more research.

S100A6 is important for cell functions and can help diagnose and treat diseases.

The protein CTCF is essential for skin development, maintaining hair follicles, and preventing inflammation.

A woman with X-linked chronic granulomatous disease developed lupus-like skin lesions, improved with treatment, suggesting a unique skin condition in carriers.

The study identified a key protein involved in producing underarm odor and found ways to inhibit it.

Inflammation may play a role in causing androgenetic alopecia.

New genetic mutations linked to rare skin disorders were found in three newborns.

Inflammation damages sweat ducts, causing sweat gland injury.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

Two new mutations in the AR gene linked to severe androgen insensitivity were found.

Certain skin proteins can form anchoring structures without the protein AMACO.

LRIG1 is linked to better survival in Merkel cell carcinoma.

Small bowel lesions in Cronkhite-Canada syndrome persist despite steroid treatment.

SFRP-4 might be an early indicator of diabetes and hypertension in men with androgenic alopecia.

Markers CRABP1, Nestin, and Ephrin B2 are present in skin cancer environments and may influence their development.

The flaky skin mouse mutation is a natural model for studying human psoriasis.

CCCA is a common, progressive hair loss condition that may not always be linked to hair care practices and requires a biopsy for diagnosis.

Mutations in the PADI3 gene may cause central centrifugal cicatricial alopecia in women of African ancestry.

BAFF-targeted therapies can reduce autoimmune disease activity, but more research is needed for precise treatments.

Sertoli cell transplants can reduce inflammation and improve sperm quality.

In alopecia areata, certain immune cells increase and express a protein linked to immune activation.

SCD-153 shows promise as an effective topical treatment for alopecia areata.