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A 73-year-old woman with Hypopigmented Mycosis Fungoides, a rare skin lymphoma, experienced disease progression despite treatment, emphasizing the need for ongoing monitoring.

Deleting the MAD2L1 gene is tolerated in certain mouse cancer models.

The skin has different types of stem cells that can repair and regenerate tissue.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

UVB exposure in human skin causes macrophages to produce more IL-10 and less IL-12, leading to immunosuppression.

Follicular mucinosis can be an early sign of aggressive mycosis fungoides.

A rare skin condition was confirmed to be associated with a specific virus in a young girl.

Stress in hair follicle stem cells causes inflammation in a chronic skin condition through a specific immune response pathway.

Treating H. pylori infection might help cure alopecia areata.

Catalytic antibodies are early indicators and active participants in the development of systemic lupus erythematosus.

Early treatment and regular check-ups are crucial for lupus patients to prevent progression and improve outcomes.

Some cases of folliculotropic mycosis fungoides may progress slowly and not need aggressive treatment.

Reflectance confocal microscopy reliably identifies skin cancer features like horizontal skin tissue sections.

Most cutaneous adnexal tumors examined were benign and resembled common skin tumors.

Myasthenia gravis can affect both motor and non-motor systems due to immune system issues.

Alopecia areata can be an early sign of Hodgkin’s lymphoma and may improve with lymphoma treatment.

Alopecia mucinosa can be treated successfully with minocycline.

Mouse models help understand alopecia areata and find treatments.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

Bariatric surgery improves ovulation rates in women with PCOS and obesity better than medical therapy.

The FDA approved the first gene therapy for a blood disorder after overcoming early challenges and demonstrating patient benefits.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Cronkhite-Canada syndrome is rare, has a poor prognosis, and requires early diagnosis and ongoing treatment.

The man was diagnosed with stage III multiple myeloma and treated to improve kidney function.

Trichoscopy can reliably distinguish between alopecia areata and trichotillomania.

DNA profiling in forensics has improved, but predicting physical traits and ancestry from DNA has limitations and requires ethical consideration.

The Spanish version of the Hair Specific Skindex-29 scale is a reliable and valid way to measure the impact of hair loss on women's quality of life.

Kidney transplant patients often have skin issues, mainly infections.

Tandem repeats significantly influence hair color, especially darker shades, across different ancestries.