Search

everythinglearnresearchcommunity

for

Search:↓

Half-siblings with a rare skin condition improved with treatment for a fungal infection, but hair loss remained.

Cronkhite-Canada syndrome can cause multiple gastrointestinal polyps and various physical symptoms.

The new method combining dermoscopy and Reflectance Confocal Microscopy is more effective for evaluating vitiligo.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

Cholesterol issues in skin and hair may cause permanent hair loss by triggering inflammation.

A new gene mutation causes vitamin D resistance and hair loss in two unrelated girls.

Trichoscopy effectively diagnoses allergic scalp contact dermatitis.

Hair follicle stem cells can become corneal-like cells, potentially helping restore vision.

Trichoscopy can help identify systemic diseases, not just hair and scalp issues.

An 11-year-old girl's hair loss was caused by a Cladosporium fungal infection, which was cured with itraconazole treatment.

Latanoprost eye drops caused excessive cheek hair growth and eyelash whitening in a woman.

A 2-year-old girl with a rare vitamin D disorder had rickets and hair loss, but treatment was ineffective due to poor compliance.

Bmpr2 and Acvr2a receptors are crucial for hair retention and color.

Kerion is a rare but serious scalp infection that needs proper treatment.

Reducing immunosuppression and using antiviral creams improved the woman's skin condition.

Retinoic acid causes gland formation instead of hair in mouse skin by altering epidermal and dermal interactions.

A specific gene mutation causes vitamin D-resistant rickets and hair loss.

KID syndrome should be reclassified as an ectodermal dysplasia.

Radiation therapy with chemotherapy can cause severe, long-lasting hair loss.

Vogt-Koyanagi-Harada disease can develop during interferon therapy for chronic hepatitis C.

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

Children with alopecia areata, especially with Down syndrome or thyroid issues, should be screened for thyroid disease.

Follicular red dots may be a normal feature seen in people with less skin pigmentation, not necessarily indicating a scalp disorder.

Rapamycin reduces age-related hearing cell loss in mice, but acarbose does not.

Adalimumab helped control a child's severe eye disease when other treatments failed.

Sporadic trichoblastic neoplasms generally don't recur or spread, with one case showing a specific genetic fusion.

Ritlecitinib provides new treatment options for diverse alopecia areata patients.

The report described a unique case of Cronkhite-Canada syndrome with unusual polyps and an association with multiple myeloma.

Tay syndrome is a unique genetic disorder causing skin, hair, and developmental issues.