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A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Hair repigmentation can indicate malignancy and should be investigated.

The condition is harmless, doesn't worsen, and needs no invasive treatment.

Localized trichorrhexis nodosa is a hair condition where hair becomes fragile and breaks easily due to damage.

A boy had a rare scalp condition with thickened skin and different-colored hair.

The newborn's skin condition improved over time, leaving only lighter skin patches.

A woman got melanoma on her scalp after anti-hair loss treatment with injections.

Surgeons should know about pilomatricoma for accurate diagnosis, even though it's rare.

A 7-year-old girl had a non-painful skin growth at her belly button, which was removed and identified as a keratinous cyst.

Complete removal of scalp tumors is crucial, but malignant cases may recur or metastasize, requiring a multidisciplinary approach and close follow-up.

Mutations in the desmoplakin gene can cause hair problems and deadly heart disease.

Hair examination helps diagnose rare neurological diseases in children.

Spiny keratoderma is a rare skin condition with small spines on palms and soles, possibly linked to abnormal hair formation.

A newborn girl has a rare skin condition with two ulcers on her buttock that are healing on their own.

Dermoscopy helped diagnose a rare skin disease which slightly improved with treatment.

A hair cyst can become cancerous, showing specific keratins from the hair sheath.

Genetic defects in the Wnt/PCP pathway may cause congenital yellow nail syndrome.

Hair matrix cysts are rare skin nodules with unique features, often needing surgical removal.

A rare hair follicle tumor was found on a woman's vulva.

A benign skin tumor was removed from a man's leg, and it didn't come back after 9 months.

Better diagnostic tools and treatment guidelines are needed for segmental vitiligo and related pigment issues.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

Early recognition and treatment of VATS in transplant patients improve outcomes.

Scalp pemphigus vulgaris can be effectively treated with low-dose prednisone and triamcinolone.

The girl has a genetic hair condition causing thin hair since childhood.

The woman has a rare skin condition called follicular Dowling-Degos disease, which has limited treatment options.

A pilomatrixoma in the eyebrow can cause hair loss and skin lightening.

Trichoscopy helps accurately diagnose Netherton syndrome, often mistaken for atopic dermatitis.