Search

everythinglearnresearchcommunity

for

Search:↓

Giant solitary trichoepithelioma is a rare, usually non-cancerous hair follicle tumor that can sometimes turn into skin cancer.

Porokeratotic eccrine and hair follicle nevus is a very rare skin disorder possibly caused by a GJB2 gene mutation.

A girl with lupus had unusually long and thick eyelashes, a rare symptom of her condition.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

Tigers had a skin condition causing hair loss and inflammation, but the cause is unknown and treatment didn't work.

Syphilis can cause hair loss and skin changes in HIV-positive patients, and proper treatment can resolve these symptoms.

Two girls experienced temporary hair loss after getting the HPV vaccine, which may be related to the vaccine.

Keratin-associated proteins may have roles in various mouse tissues, not just hair.

Trichotillomania may have a genetic link to psychiatric disorders.

A rare autoimmune condition, Satoyoshi syndrome, can start in adults and improve with immunosuppressive treatment.

The Persian cat has a skin infection caused by a fungus, treatable with antifungal medication.

Fibrosing alopecia in a pattern distribution is a unique hair loss condition that may respond to antiandrogen therapy.

Dermoscopy is crucial for diagnosing rare scalp tumors like trichofolliculoma.

Pityriasis rubra pilaris is a rare skin disorder with reddish-orange patches and thickened skin, needing better treatment understanding.

A woman's hair grew back after treatment for a rare hair loss caused by proton therapy.

It's important to consider genetic hair disorders when diagnosing hair loss.

Dermoscopic features can help identify and differentiate types of pityriasis versicolor.

Lichen planopilaris causes permanent hair loss and scarring due to damage to hair follicles and can be mistaken for other hair loss conditions.

Two siblings were found to have a genetic condition causing progressive hair loss and woolly hair, which may often be misdiagnosed.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

Older men's scalp damage increases with age and sun exposure, a baby girl in the Philippines has Schimmelpenning syndrome, and thyroid screening is advised for children with hair loss and certain risk factors.

People with late-stage HIV-1 often experience a specific type of hair loss linked to multiple factors, including nutritional issues and immune responses.

A combination of oral cyclosporin and PUVA treatment worked well for a severe skin condition called generalized pustular psoriasis.

Trichoscopy is a quick and easy way to diagnose most genetic hair problems without invasive methods.

Trichotillomania shows specific signs like black dots and uneven hair lengths but lacks certain features of alopecia areata.

TTNPB helps turn stem cells into neural stem cells, improving depression-like behaviors in rats.

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

Trichoscopy is useful for early detection and monitoring of female pattern hair loss.

Trichoscopy helps distinguish between scalp Discoid Lupus Erythematosus and Lichen Planopilaris for accurate diagnosis and treatment.

PCR-ELISA is better for identifying the fungus causing scalp infections in Ugandan children than traditional methods.