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A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Pachyonychia congenita is linked to a keratin gene on chromosome 17.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

This is the first known case of parathyroid cancer in a patient with Birt Hogg Dube Syndrome.

A rare skin growth in a baby was successfully removed without coming back.

A man had a non-cancerous neck tumor related to hair follicles removed with no return of the tumor.

The oncoprotein causes abnormal hair growth without increasing skin cancer risk.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.

Keratin 17 is important for skin's response to radiation, affecting many genes and cell division.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Skin cells can naturally limit the growth of cancerous changes by balancing cell renewal and differentiation.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

Intense pulsed light treatment mainly damages pigmented hair parts but spares stem cells, allowing hair to regrow.

A 16-year-old boy had a rare case of Becker's nevus on his face and mouth.

Herpes zoster infection can cause permanent hair color change in the affected area.

Eruptive vellus hair cysts can run in families.

Intralesional chemotherapy with 5-fluorouracil and methotrexate may worsen keratoacanthoma-type skin cancer in transplant patients.

A 70-year-old man with skin cancer on both sides of his forehead was treated with surgery and cryotherapy, highlighting the need for early detection and prevention.

The tumor on the man's nose was a rare type called pedunculated follicular hamartoma.

A rare skin lesion in a 64-year-old woman was successfully treated with a laser, showing minimal redness and no return after one month.

Truncated hHb1 keratin may play a role in breast cancer cell transformation.

p14ARF and p16Ink4a cause hair follicle stem cell aging and dysfunction.

A man had a non-cancerous, fast-growing skin lump on his arm that was removed with surgery.

High levels of ODC and a mutant Ha-ras gene cause tumors in mice.

Increasing type 17 collagen reduces aging signs in skin cells caused by UV light.

TB and BCC tumors show similar follicular differentiation patterns.

The new antibody, TYHF-1, specifically targets certain hair-related structures.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.