Search

everythinglearnresearchcommunity

for

Search:↓

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

Impaired LEF1 activation speeds up skin cell development in Hutchinson-Gilford Progeria Syndrome.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

Microorganism overgrowth and hyperkeratosis may trigger immune reactions causing lichen planopilaris.

A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.

A rare genetic disease caused severe, worsening hair loss from early childhood with poor treatment results.

KFSD is a rare condition causing scarring hair loss, with no effective treatment known at the time of the report.

A 3-year-old girl has a rare condition causing sparse hair and nail issues, with minimal improvement from treatment.

OCT can non-invasively diagnose follicular keratosis and other hair follicle disorders.

The woman's forehead lesion was caused by ointment use and resolved with treatment.

Acitretin effectively improved the woman's skin condition.

Eruptive vellus hair cysts are often missed in diagnoses.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

Bilateral ovarian hyperthecosis is a rare but treatable cause of increased facial hair in postmenopausal women.

A 16-year-old boy's arm hair grew more after wearing a splint, but it returned to normal in 8 months.

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

Matrical tumors share a common growth mechanism involving the Wnt pathway and consistent PHLDA1 expression.

The boy's skin condition improved significantly with a specific ointment after other treatments showed only mild results.

Basal cell carcinoma shows keratin patterns similar to hair follicle structures.

Nevus sebaceous is identified by unique skin changes, including thickened skin, fewer hair follicles, and many sebaceous glands.

Minoxidil can cause excessive hair growth.

Skin organoids with NCSTN mutation show changes in hair follicle development and higher inflammation, key features of Hidradenitis Suppurativa.

These ovarian conditions cause high testosterone levels.

A woman's increased hair growth during pregnancy due to PCOS resolved after delivery.

Acitretin can cause excess tissue growth and hair loss.

Trichostasis spinulosa is a rare skin condition with hair-filled plugs in hair follicles.

Without keratin 10, there's more growth and development of oil-producing skin cells.

The hairless gene mutation causes baldness by disrupting hair follicle structure.

A benign skin tumor grew quickly in a dialysis patient and was surgically removed.