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Researchers found four genes that could help diagnose severe alopecia areata early.

Zinc sulphate solution was not effective in reducing the number, duration, or severity of recurrent herpes simplex infections.

Lichen planopilaris in men often involves scalp redness and itching, with some also having hair loss, mucosal lichen planus, or thyroid disease, and treatment improved symptoms in nearly half of the cases.

Societal pressure for the perfect body leads to health risks and disorders.

Lithium can cause skin issues like acne and hair loss.

Higher antigliadin antibodies are linked to more severe alopecia areata, suggesting screening for celiac disease in these patients.

Progeria causes early aging due to a gene mutation, affecting skin, bones, and heart, with treatments aimed at improving life quality.

Early detection and multidisciplinary treatment are crucial for managing Papillon-Lefévre syndrome.

There is no significant link between metabolic syndrome and alopecia areata.

A unique case showed a rare combination of two types of lichen planus on the face.

The analysis aims to identify the most effective and safest treatments for alopecia areata.

A family was found with both Trichorhinophalangeal syndrome and Loose Anagen Syndrome, suggesting a genetic connection.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Sodium hypochlorite can effectively prevent and remove Staphylococcus aureus biofilms in atopic dermatitis at high enough concentrations.

Oral tofacitinib may be an effective and tolerable treatment for some people with severe alopecia areata.

The document says a skin condition called alopecia areata causes hair loss and stress, and is treated with strong skin creams, injections, or other therapies, but treatment success varies.

Anorexia Nervosa and Bulimia Nervosa are complex eating disorders with increasing incidence among young females, significant morbidity, and varying mortality rates, requiring more research for better treatment.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

Renal transplant recipients often have skin issues, especially infections, and need regular skin check-ups.

A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

Alopecia areata in Taiwan has a high disease burden and needs better research and diagnostic criteria.

ARWH is a rare hair disorder with no cure, but potential treatments include minoxidil and other therapies.

Combining laser treatment with steroid cream is more effective for alopecia areata than using the cream alone.

The visfatin GT genotype may increase the risk of Alopecia Areata.

These gene variations are not linked to alopecia areata in Egyptians.

Alopecia areata is a hair loss condition caused by immune factors and can be treated with JAK inhibitors.

The Middle East and Africa need better data, treatment consensus, and support for Alopecia Areata.

New research has found 14 genes linked to the risk of developing alopecia areata, improving understanding and treatment options.

An infant with a zinc deficiency skin disorder improved with zinc treatment.

People with alopecia areata have much lower Vitamin-D levels than healthy individuals.