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A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

Isotretinoin is effective for treating dissecting cellulitis, but recurrence is common.

No treatment is clearly better for central serous chorioretinopathy, and more research is needed.

Interface dermatitis is the most common skin change in drug-induced hypersensitivity syndrome.

Prevent skin tears by maintaining health, protecting skin, and ensuring safe environments.

Two siblings were diagnosed with Trichothiodystrophy, identified by brittle hair and low sulfur content.

Trichoscopy effectively diagnoses and monitors treatment in children with tinea capitis.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

CK 15, follistatin, and Bmi-1 can help differentiate basal cell carcinoma from squamous cell carcinoma.

Topical clascoterone may help treat hidradenitis suppurativa.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

A woman with inflammatory bowel disease improved after treatment with ustekinumab for a rare skin condition associated with her disease.

Early shedding of the inner root sheath in noninflamed hair follicles is a relatively specific sign of Central Centrifugal Cicatricial Alopecia.

MCTD should be considered in children with recurring muscle issues, lupus-like symptoms, and edema.

GLI1 RNA CISH effectively identifies basal cell carcinoma but is less specific for benign follicular tumors.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

Early detection and intensive treatment of diseases caused by Staphylococcus aureus toxins are crucial for reducing severe health effects.

The consensus document recommends a comprehensive treatment plan for Hidradenitis Suppurativa, including various medications, surgery, lifestyle changes, and the need for more research and resources.

A SALT score of ≤ 20 indicates meaningful improvement in alopecia areata treatment.

The MIRA technique improves cellulite treatment results and patient satisfaction.

A 4-year-old girl had a rare hair disorder affecting only part of her scalp.

A rare case of isolated trichothiodystrophy was identified, marked by brittle hair with low sulfur content.

A man with Isaac's syndrome affecting only one side of his body improved after immune system-targeted treatment.

The Turkish version of the MAIA-2 Scale is valid and reliable for patients at a dermatology clinic.

UK hair restoration surgery follows strict clinical standards.

First Korean case of Cronkhite-Canada syndrome with colon cancer and serrated adenoma.

The top research priorities for congenital ichthyosis include long-term side effects of oral retinoids, best topical treatments, and treatments for itch and hair loss.

Skin tumor cells in patients with tuberous sclerosis have higher levels of a protein called cathepsin B.

The document found differences in lesion distribution and microscopic features among trichostasis spinulosa and similar skin conditions.