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A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

The rs1128977 gene variant may affect cholesterol and body measurements.

Onyx® embolization effectively treats facial arteriovenous malformations with minimal complications.

A man got unusual crescent-shaped cuts from a laser tattoo removal due to a laser technical issue, but healed without scars.

Early diagnosis and treatment of SLE are crucial to prevent severe complications.

Changing neuroactive steroids in baby male rats affects their memory and learning differently as they grow up.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

A reliable method was developed to measure aristolochic acid-I in rat blood.

Upadacitinib improved multiple immune-related conditions in one patient.

Metaphors like "butterfly rash" and "moth-eaten" help doctors identify and describe skin conditions.

Rodent spiny hair traits are due to genetic factors other than the Edar gene.

The document reports the 19th global case of a rare skin condition in a patient from Colombia.

Statins may help treat alopecia areata by reducing harmful immune interactions.

N-WASP is essential for healthy skin and preventing inflammation.

Tranexamic acid turns white hair brown in certain mice by affecting specific proteins.

NM2 and RLC phosphorylation are essential for normal inner ear hair cell function.

The combination of mitoxantrone, etoposide, and prednisolone is effective for treating relapsed lymphoma with manageable side effects.

Early diagnosis and treatment of nail lichen planus in children can prevent permanent nail damage.

Leflunomide and anthralin may effectively treat severe alopecia areata.

Hair loss might be due to nerve issues, treatable with electric stimulation or acupuncture.

Researchers developed a method to measure different forms of a drug that could help treat prostate issues and hair loss, and found how these forms behave in animals.

MC-DNA vector-based gene therapy can temporarily treat CBS deficiency in mice.

A man developed a rare cancer on his scalp after a hair transplant possibly due to sun damage, laser effects, and inflammation.

The FOXN1 gene is crucial for developing immune cells and preventing immune disorders.

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

PAON shows skin patterns due to genetic mosaicism.

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