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DHL-HisZnNa may help reduce hair loss from chemotherapy, but more research is needed.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

A gene called HDAC9 might be a new factor in male-pattern baldness.

The TCL1 transgenic mouse model is useful for understanding human B-cell leukemia and testing new treatments.

RNase L hinders hair growth by altering immune signals.

IL-18 levels are higher in hidradenitis suppurativa patients and may indicate disease severity.

Farudodstat may effectively treat alopecia areata without harming hair follicles.

Human TMEM2 does not break down hyaluronan but helps control its metabolism.

Genetic testing can diagnose hair loss linked to DSG4 gene variants.

Consider infectious diseases like visceral leishmaniasis before diagnosing autoimmune hepatitis.

Alopecia areata patients have more activated T cells in their blood, which may help in developing treatments.

Monilethrix severity varies and may be influenced by other genetic or environmental factors.

RXRα is crucial for proper immune response and links diet to immune function.

DM and AA may share a common cause.

RNase L hinders hair follicle regeneration by altering immune signals.

Targeting TCR-Vβ2 in cutaneous T cell lymphoma shows promise for safer, more specific treatment.

Skin problems like itching, dry skin, and hair loss are more common in hepatitis C patients after interferon treatment, but lichen planus is not linked to the infection.

Hyperaesthetic leucotrichia in horses causes painful, recurring skin lesions and hair color changes, especially in Arabian and American paint horses.

Imbalance in immune cells causes hair loss in alopecia areata.

HIV patients with lower CD4 T cell counts often have more skin problems.

Early recognition of skin lesions in Birt-Hogg-Dubé syndrome is crucial for detecting renal tumors early.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

Mice with the 'lanceolate hair' mutation have abnormal hair and skin similar to human Netherton's syndrome.

A child's rare skin disease was triggered by chickenpox.

Alopecia areata involves specific immune cells, offering potential treatment targets.

PD‐L1 and PD‐L2 may not effectively control immune activation in alopecia areata.

Scalp discoid lupus erythematosus shows two distinct patterns in skin of color.

Permanent hair loss after a stem cell transplant can be a sign of chronic immune system attack on the scalp.

Hydroxychloroquine may cause false results in tuberculosis tests for patients with autoimmune skin diseases.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.