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Trypsin slows hair growth and affects color by causing cell death in hair follicles.

Eruptive vellus hair cysts are rare and often misdiagnosed, requiring biopsy for accurate diagnosis.

The study found specific hair and scalp patterns for different types of hair loss in Koreans, noting racial differences affect diagnosis.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

Skin cancer in sun-exposed areas is more likely to come back.

Trauma can cause fat inflammation and abnormal hair growth.

More research and guidelines are needed for managing prostate cancer in people with high-risk genetic mutations.

Somatic BHD mutations are rare in Japanese renal tumors.

Treatment reduced cystic lesions but didn't change existing Nevus Comedonicus.

Changing certain hairstyles can prevent worsening hair loss in Mexican women.

Different keratins in hair follicles can help identify hair tumor origins.

Female pattern hair loss is linked to genetics, family history, and lifestyle factors.

Trichogram is useful for diagnosing hair disorders, but newer, non-invasive methods like trichoscopy are becoming more popular due to their sensitivity and ability to monitor treatment responses.

A family had a genetic condition causing hair loss on the scalp, passed down through four generations.

Dermoscopy helped diagnose a rare hair disorder in a 2-year-old boy.

A man's rare adrenal tumor caused feminization and white hair, was removed surgically, and improved after treatment.

EGFR inhibitors can cause unusual localized hair growth.

A two-step method was created in 2015 to make more cells that help with hair growth, but they need to be combined with other cells for 4 days to actually form new hair.

Exclamation mark hairs help distinguish syphilitic alopecia from alopecia areata.

Trichoscopy helps diagnose hair and scalp problems but isn't always definitive and should be used with other methods.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

A woman's symptoms of increased body hair and testosterone were caused by a rare adrenal tumor, which was removed successfully.

The antibody created from BCC tissues reacts similarly to both BCC and hair follicles, suggesting BCC may come from hair follicle cells.

Different treatments are effective for hair loss conditions, but results vary by individual factors.

Colorectal cancer's ability to spread is due to changes in many genes, not just one.

Non-melanoma skin cancer in darker-skinned people can be misdiagnosed, so doctors need to be more aware to diagnose it correctly and early.

The man died from lung cancer, not the rare nail tumor.

CCCA may be a fibroproliferative disorder, and anti-fibrotic therapies could help.

A child was initially wrongly diagnosed with a fungal scalp infection but actually had a non-scarring hair loss condition called Temporal Triangular Alopecia.

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.