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A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

Hair follicle stem cells can become corneal-like cells with the right environment.

Trichofolliculoma is a rare skin bump on the face or scalp.

Trichoscopy is crucial for diagnosing rare genetic hair disorders.

Laser hair reduction near the eyebrows can cause serious eye injuries even with safety measures.

Inactivating β-catenin is essential for chick retina regeneration.

A 5-year-old girl with a rare genetic disorder, lipoid proteinosis, showed reduced new lesions but persistent scars after avoiding skin trauma.

Dermatoscopy can help identify hydroquinone-induced skin issues, avoiding invasive biopsies.

A woman had a unique skin growth with hair follicle, oil glands, fat cells, spindle cells, and nerve fibers.

Congenital atrichia with papular lesions causes permanent hair loss and skin bumps due to a gene mutation.

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

Good preoperative assessment is crucial for safe and effective eyelid and brow cosmetic surgery.

Localized dystrophic epidermolysis bullosa (DEB) can lead to scarring alopecia, highlighting the need to recognize and address this complication.

A rare skin condition usually found near the eyes was found on a farmer's scalp.

Shiny white structures in trichoscopy can indicate long-standing discoid lupus erythematosus alopecia.

The boy's genetic diagnosis of ectodermal dysplasia helped improve management and counseling for him and his sister.

Trichogerminoma is a rare, benign skin tumor from hair cells, with a small risk of becoming cancerous.

Latanoprost eye drops caused excessive hair growth and eyelash whitening in a woman.

Recognizing bamboo hair helps diagnose Netherton’s syndrome.

Coinheritance of BRCA2 and CYLD genes may lead to new treatment options for certain cancers.

A young man's cheek papule was identified as a benign hair follicle tumor using a skin surface microscope.

A baby with a skin condition improved with treatment but developed a rare form of the condition affecting only his trunk.

The study found that pili bifurcati causes hair to intermittently split into two branches, each with its own outer layer.

An infant with Hutchinson-Gilford Progeria Syndrome had successful surgery to fix breathing issues caused by a new genetic mutation.

A 10-year-old boy was diagnosed with a rare scalp condition causing hair loss and treated with a topical cream.

Hair follicle stem cells can become corneal-like cells, potentially helping restore vision.

Systemic mastocytosis may cause a type of hair loss called cicatricial alopecia.

Bardet-Biedl syndrome may include under-recognized skin problems related to its metabolic disturbances.

Reflectance confocal microscopy confirms that yellow dots are signs of damaged hair follicles in alopecia areata.