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Ritlecitinib is safe and well-tolerated for treating alopecia areata in patients aged 12 and older.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

DPR can show different hair characteristics, as seen in two brothers with normal hair.

Genetic analysis is crucial for diagnosing ectodermal dysplasia syndromes, and new therapies may help improve skin issues.

Riboflavin deficiency in baby pigs causes health issues, and while supplements help, they may not fully fix internal problems.

The study suggests a link between varicella-zoster virus and segmental vitiligo, with evidence of the virus disrupting skin pigment cells.

High-dose mizoribine effectively controls symptoms in adolescents with lupus while reducing steroid use, with manageable side effects.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

Early diagnosis and biotin treatment are crucial for infants with biotinidase deficiency to prevent severe complications.

The boy's symptoms improved with vitamin C treatment, highlighting the need to consider scurvy in kids with unusual diets.

A new mutation caused a rare hair disorder in a Polish girl, not inherited from her family.

A 12-year-old boy had severe shingles and skin damage after a stem-cell transplant.

A mutation in the IKZF1 gene causes immune system overactivity, linked to autoimmune diseases like lupus.

A 16-year-old girl's skin rash was likely caused by an infection and improved with topical steroids.

Abrocitinib, a JAK inhibitor, may help treat atopic dermatitis and alopecia universalis together.

Skin can produce blood cells, often due to disease, which might lead to new treatments for skin and blood conditions.

Skin symptoms could help in early COVID-19 diagnosis but more research is needed to confirm their reliability.

The patient's hair loss from alopecia totalis returned despite initial successful treatment.

The hepatitis B vaccine did not cause hair loss in the tested mice.

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

An antibiotic called co-trimoxazole can effectively treat autoimmune diseases.

An extremely low-birthweight infant had a rare genetic skin disease and died despite treatment.

A rare skin infection in a 10-year-old kidney transplant patient was successfully managed by adjusting medication.

An 8-year-old girl with vitiligo developed extra hair growth on her knee after using tacrolimus ointment.

Blood and urine markers are important for diagnosing lupus in children.

The skin condition Ulerythema ophryogenes did not improve with treatment in a patient with other birth defects.

Constant light exposure during pregnancy changes newborn rabbits' skin, affecting hair follicles, skin thickness, and pigment cells.