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An elderly woman's upper lip lump, thought to be a mucocele, was actually a rare type of lymphoma usually found on legs, treated successfully with chemotherapy and radiation.

mHa2 and mHa3 keratins have different structures and roles in mouse hair and tongue tissues.

Male-to-female skin grafts in mice are rejected due to sex-linked antigens.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

Three new gene mutations cause rickets and hair loss, treatable with high calcium and calcidol, but hair regrowth is rare.

Delta1 is crucial for controlling skin cell growth and preventing tumors in mice.

The HSD3B1 variant increases hair loss risk in overweight women with PCOS.

Dandruff is linked to changes in the immune system of hair follicles and skin.

Vitamin D receptor FokI gene variation is not linked to alopecia areata.

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

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

Trichohyalin may trigger the immune response causing alopecia areata.

Graft-versus-host disease is a complication where donor immune cells attack the recipient's body, often affecting the skin, liver, and gastrointestinal tract.

A specific gene mutation in Japanese people can cause varying degrees of hair thinning in adulthood.

Adalimumab significantly improves quality of life for patients with moderate to severe hidradenitis suppurativa.

CD2 might be a new treatment target for patchy alopecia areata.

Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

Farudodstat may effectively treat alopecia areata by protecting hair follicles without harmful effects.

A specific mutation in PA-PLA1α causes abnormal hair growth.

The DNMT3B -579G>T polymorphism may increase the risk of colorectal cancer.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

A gene mutation in mice causes permanent hair loss and skin issues.

Dupilumab effectively treats severe skin issues in a rare genetic disorder.