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Title change to "Central Centrifugal Cicatricial Alopecia (CCCA)"; common in African American women; hair-grooming methods may contribute; no effective therapy found; trials needed.

Baricitinib may reactivate trichilemmal cysts in people with a history of these cysts.

MRI can show unusual brain changes in adrenomyeloneuropathy.

Certain miRNAs might be involved in a hair loss condition called frontal fibrosing alopecia and could possibly help in its diagnosis.

Various potential triggers may be causing the rise in frontal fibrosing alopecia, and avoiding these could help stop the disease's increase.

Alopecia areata may involve disrupted mesenchymal function in hair follicles.

Steroid treatment improved both gut and nerve symptoms in a man with Cronkhite–Canada syndrome.

Scalp disease in dermatomyositis causes significant symptoms and has unique features.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

Lichen planopilaris is the most common type of scarring hair loss observed, with a variety of symptoms and tissue changes.

Milia may come from the outer part of the hair follicle.

Sarcoidosis can mimic other skin disorders, making diagnosis challenging.

Hair splitting and nail detachment are linked conditions.

Hair breakage may be an early sign of a hair loss condition called CCCA in African American women.

Certain medications and patient factors increase the risk of Intraoperative Floppy Iris Syndrome during cataract surgery, but with careful planning and technique adjustments, complications can be minimized.

Targeting specific metabolic and ionic pathways may improve alopecia areata treatment.

IFAP syndrome is a rare genetic disorder causing skin, hair, and eye issues, with limited treatment options.

Vogt-Koyanagi-Harada disease affects vision and skin, mainly in people with darker skin, and is treated with steroids and immunosuppressants.

Eyelash transplantation can cause eye damage and pain if not done carefully.

A mutation in the SREBF1 gene causes both hereditary mucoepithelial dysplasia and IFAP syndrome, which are related conditions.

Certain factors can trigger hormonal imbalances and cyst formation, leading to Polycystic Ovarian Syndrome (PCOS).

Rat hair follicle stem cells can become corneal epithelium-like cells when exposed to rabbit corneal limbal stroma.

Surgical removal of eyelid mass showed it was non-cancerous, with no recurrence after one year.

Schimmelpenning Syndrome requires careful evaluation and tailored treatment for skin, eye, and developmental issues.

Potential therapeutic targets for scarring hair loss are identified.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

Rituximab may be an effective treatment for Cronkhite-Canada syndrome with kidney disease.