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A new severe form of monilethrix syndrome includes hair loss, scalp itching, cataracts, and distinct facial features.

Polarizing light microscopy can easily and reliably diagnose congenital keratinizing disorders like Netherton syndrome.

Nagashima-type palmoplantar keratosis in Asians is caused by a SERPINB7 gene mutation.

A rare skin condition with cysts was found on a 5-year-old boy's scalp.

Molluscum contagiosum can occur in epidermoid cysts, especially with prolonged steroid use.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

A new gene mutation linked to a skin condition was found in a Spanish family.

Mutations in the KLHL24 gene cause a skin disorder in some Russian families.

A 16-year-old boy's facial condition improved with doxycycline, suggesting an immune response to hair follicle damage.

Removing anthrax toxin receptor 1 in pigs prevents Senecavirus A infection and causes a rare disease similar to GAPO syndrome.

Vogt-Koyanagi-Harada disease can develop during interferon therapy for chronic hepatitis C.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

NSC167409 can effectively inhibit the virus causing hand, foot, and mouth disease.

Biliverdin IXβ and IXδ help Pseudomonas aeruginosa adapt to chronic infections.

Skin cells might help spread prion diseases like Creutzfeldt-Jakob disease.

Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.

Two siblings have a rare hair condition caused by a new genetic variant.

The hair keratin variant is mostly found in Caucasians.

A rare gene variant causes hair and nail issues in a family.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

New mouse models of Pemphigus show severe symptoms and need better treatments.

Genetic factors alone might not cause pemphigus vulgaris; other factors like birth complications and puberty may trigger it.

A boy's scalp infection, usually found on the body, was effectively treated with antifungal cream.

Scalp pemphigus vulgaris can be effectively treated with low-dose prednisone and triamcinolone.

A woman had meningitis caused by mixed connective tissue disease, not an infection.

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

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.