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The PROCLIPI study found markers that help predict outcomes in skin lymphoma patients.

LC-OCT is an effective new method for diagnosing classic lichen planopilaris.

Black women with CCCA are more likely to have uterine fibroids.

Cutaneous lupus erythematosus is a chronic skin disease that can progress to systemic lupus in some cases and requires treatment to prevent recurrences and scarring.

Chronic cutaneous lupus erythematosus causes scarring, hair loss, and skin discoloration, especially on sun-exposed areas.

CCCA is a common, scarring hair loss in Black women that needs early detection.

CYLD mutations cause a variety of skin tumors with symptoms starting around age 16, and treatments are currently limited.

Estrogen and MLL enzymes work together to regulate genes important for hair growth and leukemia.

CXCL7 is essential for muscle repair by aiding early neutrophil infiltration.

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

The LGBTQ+ STEM @UCL Network helps increase visibility and support for LGBTQ+ individuals in STEM at University College London.

The 2012 SLICC criteria provide an updated method for classifying Systemic Lupus Erythematosus.

A patient with Cronkhite-Canada Syndrome developed colon cancer that spread to the liver, showing the need for regular cancer checks in such patients.

A novel CLDN1 mutation in a 2-month-old with NISCH showed improvement with symptom management.

The document concludes that treatment for cutaneous T-cell lymphoma should be customized to each patient's disease stage, balancing benefits and side effects, with no cure but many patients living long lives.

Mutations in claudin-1 and claudin-3 cause hair loss in baby mice.

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 Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

HTLV-1-associated lichenoid dermatitis (HALD) is linked to an immune response against HTLV-1-infected cells.

Nε-(carboxymethyl) lysine delays hair growth by blocking a key protein.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

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

CLK1 is needed for skin cells to become epidermal cells but not sebocytes.

Nε-(carboxymethyl) lysine delays hair growth by blocking a key protein.

Topical IKKα inhibitors may help prevent CCS tumours.

Clascoterone is safe for the heart, even at high doses.