Search

everythinglearnresearchcommunity

for

Search:↓

The new classification system for skin disorders emphasizes the importance of understanding a patient's awareness of their condition for better treatment.

SCD-153 shows promise as an effective topical treatment for alopecia areata.

Most patients experienced mild to moderate skin problems during a trial for a desmoid tumor treatment.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

Accurate diagnosis and early specialist referral are crucial for managing 46,XY Disorders of Sex Development.

Hypertrichosis (excessive hair growth) can help diagnose superficial epidermolytic ichthyosis.

Topical ceramide treatment partially improves the skin condition in Jack Russell Terriers with a genetic skin disorder.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

Blocking CISD1 reduces hearing loss from cisplatin in mice.

Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.

Patients with Shwachman-Diamond syndrome often get misdiagnosed due to a wide range of symptoms, including immune system problems and bone abnormalities.

Patients with Complete Androgen Insensitivity Syndrome need psychological support and multidisciplinary care for complex treatment decisions.

Centrifugal forces can help prepare hair follicle germs for hair regeneration.

JAK/STAT1 pathway causes hair loss during chemotherapy by reducing Shh in hair follicles.

Prednisone treatment helped a woman with Cronkhite-Canada syndrome recover from hair loss and digestive issues.

The cat fully recovered after treatment and showed no further symptoms.

Using Selenium Disulfide shampoo weekly helps prevent scalp dermatitis flare-ups.

Cronkhite-Canada syndrome causes chronic diarrhea and has a poor prognosis despite treatment.

Secukinumab reduces immune activity in hidradenitis suppurativa skin.

AIRE-deficient rats developed severe autoimmune disease similar to APECED, useful for testing treatments.

A man with Cronkhite-Canada syndrome had all 20 nails detach but improved with treatment.

Familial dyskeratotic comedones are a rare, inherited skin condition that is hard to treat but may improve slightly with topical retinoids and urea cream.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

Infliximab improved skin and bowel symptoms in Crohn's disease but caused side effects and the disease returned after stopping treatment.

IRS premature desquamation is not unique to CCCA and occurs in various scarring alopecias.

A young woman with a rare fungal infection showed significant improvement after treatment with antifungal medication.

Intralesional steroid injections can effectively treat calcinosis and ulcers in scleroderma.

Surgical excision is the best treatment for SCC, but intralesional cidofovir might be a good alternative.

Cronkhite-Canada syndrome can be diagnosed without gastrointestinal polyps if there is severe mucosal atrophy and edema.