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Higher disease activity in systemic lupus erythematosus is strongly linked to more internal organ damage.

lncRNAs may regulate hair follicle development in Hu sheep.

Sirolimus and propranolol may reduce abnormal cell growth and improve lymphatic malformations in children.

People with lichen planopilaris often have seborrheic dermatitis, which can delay the diagnosis of lichen planopilaris.

Radiesse is a versatile facial injectable used for cosmetic improvements and long-term collagen production, with careful dosing needed to prevent complications.

Laser hair removal improves quality of life but emotional benefits decrease over time, suggesting more treatments are needed for lasting effects.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

Patients with RASopathies are at risk for autoimmune disorders and should be routinely screened.

Thicker hair grows faster; hair loss patients have slower growth.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

A 46-year-old man showed symptoms of a rare condition usually seen in postmenopausal women, highlighting the need for dentist-dermatologist collaboration.

New LPA receptors (LPA4, LPA5, LPA6) have diverse roles in the body.

Digital gangrene can be an early sign of late-onset systemic lupus erythematosus.

Sry may regulate fatty acid metabolism and shows different expression levels in rat tissues.

Linoleate deficiency in rats reduces growth and n-6 polyunsaturate accumulation, causing mild symptoms.

Sertoli-Leydig cell tumors are rare ovarian tumors that can cause symptoms like menorrhagia.

Ritlecitinib effectively treats alopecia areata with manageable side effects.

A 68-year-old woman with lupus and blood disorders improved after increased steroids and immunoglobulin treatment.

Lichen planopilaris mostly affects women with fair skin and can look different on each person, needing early treatment to prevent hair loss.

A 59-year-old woman was diagnosed with a rare hair loss condition called lipedematous alopecia.

Chronic scarring alopecia is common in SLE patients and needs early detection and management.

A(1-7) treatment reduces symptoms of lupus in mice.

Patients with Bohring-Opitz syndrome and ASXL1 mutations need regular kidney ultrasounds to check for tumors.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Lupus is a complex disease that requires personalized treatment because it varies greatly between individuals.

A 61-year-old Filipino man had a skin condition that looked like another disease, making diagnosis difficult.

The DLQI is a key tool for measuring quality of life in dermatology.

A kidney transplant patient developed leprosy, likely due to immunosuppression and genetic factors, and improved with treatment.