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A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

A woman had both Graham Little-Piccardi-Lassueur syndrome, causing hair loss, and complete androgen insensitivity syndrome, making her genetically male but physically female. This suggests androgens don't affect the hair loss condition.

A young man was diagnosed with a rare hair loss condition usually seen in older women.

A painless cheek lump was misdiagnosed but found to be a rare, benign skin lesion called pilomatrixoma, treatable by surgery.

Erk signaling helps zebrafish fins regrow to the right size by using memory of the original size.

The junction of the inner and outer prepuce with good blood flow is best for vascular pedicle flaps.

The case shows how hard it is to tell apart Multiple Autoimmune Syndrome from other similar autoimmune conditions, but correct diagnosis is key for treatment to work.

Recognizing rare causes of MASLD is crucial for effective treatment and preventing complications.

Exclamation mark hairs help distinguish syphilitic alopecia from alopecia areata.

A woman with Parry-Romberg syndrome developed new curly hair on one side of her scalp, a condition not previously linked to the syndrome.

Collagen XXII is a marker for tissue junctions, aiding in structural integrity and found in muscles, heart, skin, and arthritic joints.

Lipedema is a painful fat disorder in women that's hard to treat, often worsens with hormonal changes, and requires symptom-focused therapies.

Variants in the CCDC47 gene are linked to trichohepatoneurodevelopmental syndrome.

A rare skin disorder, nevus comedonicus, can appear on one side of the body following Blaschko's lines.

Boreal caribou in northeastern British Columbia have significant health issues, including infections, tick infestations, and mineral deficiencies.

Epidermal nevi are skin cell clusters linked to various syndromes.

Alopecia areata patients show unique protein activity patterns, suggesting imbalanced signaling pathways.

Three molecular subtypes of advanced skin T-cell lymphoma were identified, with potential biomarkers for predicting treatment response and disease progression.

Tumid lupus erythematosus can cause non-scarring hair loss on the scalp and requires careful diagnosis.

CARASIL, a rare genetic disorder, was confirmed in an Arabic woman, highlighting its rarity and need for stroke prevention.

Cutaneous lupus patients have higher levels of certain immune cells in their blood and skin.

A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

JAK inhibitors may help treat certain types of hair loss, but more research is needed.

People with lichen planus are more likely to have dyslipidemia, especially higher triglyceride levels.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

Gel 2, with shark liver and borage oil, is effective for reducing inflammation and healing wounds.

A condition with certain scalp changes may come before acne keloidalis nuchae and other similar hair loss disorders.

Adults with Tatton-Brown-Rahman syndrome may have serious heart problems and need lifelong heart monitoring.