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A new severe form of monilethrix syndrome includes hair loss, scalp itching, cataracts, and distinct facial features.

Skin tumors with CYLD cutaneous syndrome show more NF-κB activity and less organized collagen.

Msx2-deficient mice experience irregular hair growth and loss due to disrupted hair cycle phases.

Certain genetic changes in the KRT82 gene may cause patchy skin in New Zealand rabbits.

Keloid skin disorder involves abnormal fibroblast activation and immune response, linked to a group of genes including FGF11.

A rare ear-area hair cyst was successfully removed from a 10-year-old boy.

Specific keratin gene mutations can cause monilethrix.

Junctional proteins stabilize the inner root sheath and connect the companion layer in human hair.

MOF controls skin development by regulating genes for mitochondria and cilia.

Calcium hydroxide in an ayurvedic product caused hair breakage.

Tight cornrow braids may cause hair loss.

A 23-year-old Syrian woman has two rare hair disorders, and avoiding hair treatments plus using vitamins and minoxidil may help.

Sphynx cats have abnormal hair follicles and keratinization affecting their skin.

A new technique effectively treats and diagnoses eruptive vellus hair cysts without recurrence.

Stem cells help remove dead cells to keep tissues healthy by balancing cell replacement and clearance.

Radiation therapy in breast cancer patients changes gene expression related to DNA damage, fibroblast growth, and hair follicle development, which could help improve treatment for radiation-induced fibrosis.

Different types of skin cells are organized in a special way in large wounds to help with healing and hair growth.

Intralesional therapy for keratoacanthoma is effective and has fewer side effects than systemic treatments.

Loss of Msx2 function causes eye development issues similar to Peters anomaly.

Histopathological examination is crucial to avoid misdiagnosis and ensure proper treatment for skin lesions.

Keratin fibrils in hair form and stop growing at specific points in the follicle.

Trichilemmal keratinization is a unique process in hair follicles where the outer root sheath turns into keratin without a specific layer.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

Aryl hydrocarbon receptor overexpression found in miniaturized hair follicles in female hair loss.

A specific DNA region controls skin cell gene expression by working with certain proteins.

A woman with Parry-Romberg syndrome developed new curly hair on one side of her scalp, a condition not previously linked to the syndrome.

EGFR deficiency in skin causes hair follicle issues and inflammation.

SVpgC2a cells show abnormal growth and keratin changes, modeling early cancer development.

Basal cell epithelioma resembles fetal hair follicles, not adult or fetal skin.

Recognizing both trichostasis spinulosa and eruptive vellus hair cysts together is crucial for accurate diagnosis and treatment.