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Psoriasis patients did not show more brain atrophy or small vessel disease than controls, but longer psoriasis duration was linked to more brain atrophy.

Systemic sclerosis skin shows varied gene patterns, suggesting potential for personalized treatment.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

Trichohyalin in sheep hair follicles may help with structure and calcium binding.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Sorafenib may cause hair loss in a way similar to alopecia areata.

The FAT1 gene and its variations can help improve wool quality in Chinese Merino sheep through selective breeding.

PRP can improve hair growth in people with hair loss, but more research is needed.

MSUD patients need careful monitoring of amino acids and zinc to prevent severe symptoms.

Psychosis can be an early sign of neuropsychiatric lupus, treatable with tailored medication.

Ruxolitinib may effectively treat APS-1 by reducing harmful immune responses.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

CENPV, a new partner of CYLD, helps regulate ciliary acetylated tubulin and is overexpressed in certain skin tumors.

A baby had a rare condition with abnormal blood vessels in the brain and unusual skin and hair growth, possibly a new syndrome.

Mice with the ab gene have abnormal sebaceous gland development, affecting sebum production.

A specific RNA, circNlgn, contributes to heart damage and scarring caused by the cancer drug doxorubicin.

Sox13 is a marker for early hair follicle development but not essential for skin and hair growth.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

Parry–Romberg Syndrome can involve the brain even without obvious symptoms, and a new diagnostic framework is suggested for early detection.

Lower GPX4 mRNA levels are linked to higher disease activity and symptoms in lupus patients.

Certain astrocytes can protect the brain and improve recovery after a stroke, and a hair loss drug might reduce cancer spread.

ARL15 is important for fat cell development and the release of the hormone adiponectin.

HLD10 can include increased body hair and Mongolian spots.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Recognizing CVG can help diagnose systemic amyloidosis early.

New protein changes may be involved in the immune attack on hair follicles in alopecia areata.

Elevated granulysin levels may indicate disease activity in vitiligo and alopecia areata.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

The prolactin gene polymorphism doesn't affect cashmere quality in these goats.

Trichodysplasia spinulosa is a rare skin condition linked to weakened immune systems, mostly in organ transplant patients.