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A runner developed tangled armpit hairs from shirt friction, preventable by shaving or wearing smooth shirts.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

The A-T advancement flap is a safe and effective method for scalp reconstruction after basal cell carcinoma removal.

Early involution in Hirosaki hairless rats' mammary glands is linked to a unique modification of STAT5A.

Degenerative changes in the lower cervical spine are common in patients with abnormal scalp sensations, with some improvement seen using pain medication and physical therapy.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

Isotretinoin can cause rare scalp cysts and hair loss, treatable with medication.

Rhupus is a complex syndrome that combines rheumatoid arthritis and lupus, making diagnosis challenging.

Cantú syndrome may be linked to pituitary adenomas.

Abrocitinib shows promise for treating various skin conditions beyond atopic dermatitis.

The guideline recommends using specific drugs and surgery together for treating hidradenitis suppurativa effectively.

A rare scalp condition, cutis verticis gyrata, was found in a woman with primary scarring alopecia.

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

Switching between the medications tofacitinib and baricitinib can be effective for treating hair loss in alopecia areata.

A young woman's Cronkhite-Canada syndrome improved on its own after she gave birth.

A healthy woman got a chest abscess from a fungal infection after gallbladder surgery, which was treated but caused temporary hair loss due to the antifungal medication.

Janus kinase inhibitors are effective for severe alopecia areata, promoting hair regrowth.

Scalp cooling effectively prevents severe hair loss in breast cancer patients treated with docetaxel and is safe.

Tocilizumab might be an effective treatment for COVID-19.

Skin tumors with CYLD cutaneous syndrome show more NF-κB activity and less organized collagen.

Managing rare genetic diseases like osteogenesis imperfecta and Escobar syndrome is complex and requires both medical and surgical treatments.

A woman with dermatomyositis improved after treatment for neck panniculitis, suggesting similar treatment for related conditions.

A young woman had a rare skin reaction to a medication for her joint disease, and a combination therapy improved her condition.

Cronkhite-Canada syndrome is a rare, non-inherited condition causing various symptoms like polyps, hair loss, and weight loss.

AQB reduces harmful skin changes in systemic sclerosis.

cGVHD often severely affects the skin, causing rapid aging and other issues.

The best concentration of triamcinolone acetonide for treating alopecia areata is still unclear.

CTHRC1 helps sweat glands recover by rebuilding nearby blood vessels.