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All parts of the CLASI-A score are important for assessing skin activity in cutaneous lupus erythematosus.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

VDC-1101 shows potential as a treatment for canine cutaneous T-cell lymphoma.

The LEF-1 gene in cashmere goats was successfully cloned and analyzed, showing potential for improving cashmere production.

Identifying nonclassic congenital adrenal hyperplasia and carriers of CYP21 mutations is challenging, and genetic counseling is recommended due to their prevalence.

Clindamycin-loaded nanoparticles effectively treat MRSA-infected wounds and promote healing.

ECCL should be considered in patients with specific skin and eye lesions.

CCCA and lichen planopilaris have similar histological features, making them hard to distinguish.

Clouston's syndrome is a rare disorder affecting nails, hair, teeth, and skin, caused by a gene mutation, and currently has no treatment, only supportive care.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

The A allele of the C2 gene increases the risk of lupus, while the G allele may protect against it.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

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

CTIP2 may help in skin development and maintenance.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

FGF22 helps hair follicle stem cells grow and develop.

CCCA is a common hair loss condition in African American women, often inherited and influenced by hairstyling, with unique scalp features detectable by special tools.

Cats likely have a reactive skin condition, while dogs may have a more complex, possibly cancerous one.

The study concludes that certain domains in Clostridium histolyticum enzymes are structurally unique, bind calcium to become more stable, and play distinct roles in breaking down collagen, with potential applications in medicine and drug delivery.

Cholecystokinin may help reduce skin inflammation in psoriasis.

Cadmium chloride pollution can cause skin disorders, speed up aging, and prevent hair growth.

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.

Higher levels of CCL7 are linked to more severe hair loss in alopecia areata patients.

CCCA causes progressive hair loss in Black women, starting from a central scalp patch.

LRIG1 is linked to better survival in Merkel cell carcinoma.

Researchers discovered how to control Claudin expression in cells, aiding cancer and regenerative medicine research.

An elderly woman's upper lip lump, thought to be a mucocele, was actually a rare type of lymphoma usually found on legs, treated successfully with chemotherapy and radiation.

Claudin 6 is crucial for normal skin and hair development.

The C-CAT tool helps assess and improve treatment for central centrifugal cicatricial alopecia.

A rare case of Cushing's syndrome and pheochromocytoma requires careful re-evaluation to avoid complications.