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A rare skin condition was found in a Labrador retriever outside North America.

Cutaneous keratocyst and steatocystoma should be called "sebaceous duct cyst" due to their similarities.

Recognizing perinevoid alopecia and concentric regrowth is important for diagnosing and treating alopecia areata.

ODC expression in mouse skin and tumors is varied and can be inhibited by retinoic acid or cycloheximide.

The hair defect is due to abnormal inner root sheath keratinization.

A Persian cat had a rare skin condition that didn't improve with treatment.

Early diagnosis and treatment can reduce cicatricial alopecia in middle-aged individuals, especially females.

This type of hair loss is probably often missed and treatments reducing inflammation might work well.

Outer root sheath cells consistently express certain keratins influenced by their environment.

Pilomatricoma is a rare, harmless skin lump that needs accurate diagnosis and timely treatment.

A rare type of skin cancer on the scalp can be mistaken for hair loss, causing delayed diagnosis and severe damage.

Cronkhite-Canada syndrome may be more treatable and less severe than previously thought.

A girl with a rare skin condition improved after one month of treatment with acitretin.

Cronkhite-Canada Syndrome often leads to death within 6-18 months.

A woman's rare benign eyelid tumor was correctly identified through detailed tissue analysis.

A rare scalp tumor was removed from a 49-year-old woman, with a good outlook if benign but needing careful monitoring if malignant.

Early diagnosis of trachyonychia improves treatment and reduces psychological and cosmetic issues.

Basal cell carcinoma shows keratin patterns similar to undifferentiated hair follicle cells.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

Keratosis pilaris is a common skin condition causing a bumpy texture, sometimes linked to other diseases, with various treatments available.

New treatments targeting specific genes show promise for treating keratin disorders.

The girl has a genetic hair condition causing thin hair since childhood.

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

Mutations in keratin genes cause cell fragility and various skin disorders.

The study found unique skin changes in a rare type of alopecia linked to a skin condition called linear morphea.

Follicular dystrophy in immunocompromised patients may be linked to medication or viral factors and can improve with treatment changes.

A 62-year-old woman with hair loss and scalp itching was diagnosed with lichen planopilaris, treated initially with topical corticosteroids, and other possible treatments include systemic steroids, antimalarials, and more.

EGFR and mTOR inhibitors may help manage Olmsted syndrome symptoms.