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Odontogenic keratocysts are caused by abnormal Hedgehog signaling and can lead to tooth and bone issues.

Removing Ctip2 in skin cells causes skin inflammation similar to atopic dermatitis.

Basal-cell epitheliomas and the pilosebaceous tract share a unique keratin, distinguishing them from other skin areas.

Harlequin ichthyosis involves abnormal skin cell structures and giant mitochondria, affecting skin and hair.

Skin debridement and antifungals successfully treated severe scalp infection without scarring.

Lipin-1 is important for skin cell differentiation and skin barrier function.

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

A 93-year-old woman developed a rare scalp condition after therapy, which improved with steroids, not antibiotics.

Keratins K1 and K10 are found in the inner root sheath and cuticle of human hair follicles.

Traumatic anserine folliculosis is a skin condition caused by friction, treatable with topical cream and avoiding trauma.

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.

Keratin proteins are increasingly recognized as important for cell health and are linked to many diseases.

Genetic testing can help diagnose skin conditions but needs more research for full effectiveness.

Seborrheic keratoses may partly come from hair follicle cells.

Keratin proteins in epithelial cells are dynamic and crucial for cell processes and disease understanding.

Papular acantholytic dyskeratosis of the vulva is a rare, benign skin condition that can be managed conservatively.

Most U.S. keratinocyte carcinoma patients are older white males living in urban areas.

Cathepsin E is crucial for normal skin cell differentiation and development.

The study found that males with KFSD had severe skin and eye symptoms, while female carriers had milder symptoms.

Different parts of the nail express different keratins, showing unique patterns of differentiation.

Topical tacrolimus can effectively treat erosive pustular dermatosis and related hair loss.

Keratin 14 may be an autoantigen in autoimmune skin diseases.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

The TRPV3 channel structure changes linked to severe itch and hyperkeratosis were identified using cryo-EM.

A rare scalp condition was successfully treated with specific medications after 9 months.

Reptile skin hardens by layering beta-proteins on keratin.

A woman got a scalp condition from using latanoprost, but it improved after stopping the drug and starting other treatments.

Mutations in keratin genes can cause skin and mucosa disorders.