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KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

The study found that it's hard to tell the difference between two types of hair loss, alopecia areata and telogen effluvium, by looking at symptoms and tissue samples.

PEH in vulvar LS is common and needs careful diagnosis to avoid confusion with cancer.

Machine learning can predict symptoms and quality of life in chronic skin disease patients using smartphone app data, and shows that app use varies with patient characteristics.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

Perifollicular erythema can indicate active frontal fibrosing alopecia.

A 17-year-old with Netherton syndrome has dry, itchy skin, brittle hair, and high IgE levels, treated with antihistamines and emollients.

Bullous pemphigoid can look like erythema multiforme, so awareness is needed for proper treatment.

New genetic mutations linked to rare skin disorders were found in three newborns.

Researchers found that dissecting folliculitis of the scalp is linked to obesity, severity increases with duration and number of nodules, and early treatment is important to prevent scarring.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Baseline severity and relapse history affect alopecia areata treatment and recurrence.

European guidelines recommend regular eye and ear exams, skin care, vitamin D supplements, and cautious use of medications for managing congenital ichthyoses.

Lower MC2R expression may contribute to alopecia areata.

EGFR signaling is essential for ear cell regeneration in both birds and mammals.

A new test using NOS2 and CCL27 genes can better diagnose and treat psoriasis and eczema.

Targeting the narrowest part of the anterior chamber angle may help prevent pupil block in glaucoma.

Recognizing perinevoid alopecia and concentric regrowth is important for diagnosing and treating alopecia areata.

Trichoscopy is a useful tool for diagnosing different hair and scalp diseases by their unique visual features.

Clq deficiency is linked to systemic lupus erythematosus symptoms.

Alopecia areata mainly affects young people, often showing as patchy hair loss on the scalp.

The symptoms described align more with Haberland syndrome, not Delleman-Oorthuys syndrome.

Two elderly men developed scalp inflammation after using a gel for skin lesions, which healed with treatment except for some permanent hair loss.

Surgery on a baby with a skin disorder improved eyelid position and eye health.

Generalized trichoepitheliomas with alopecia may indicate myasthenia gravis.

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

Deep phenotyping helps distinguish between xeroderma pigmentosum and trichothiodystrophy, aiding in diagnosis and treatment.

CTE can distort results in hair growth trials, so exclude it carefully.