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A young child with alopecia areata and psoriasis improved with treatment, suggesting a link between the two conditions.

Psoriasis is a common, genetically influenced skin disease worsened by stress and lifestyle, but targeted treatments are promising.

Laser hair reduction can sometimes cause a rare skin condition called Fox-Fordyce disease.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

Melanoma risk tools need improvement, a gene mutation causes a hair disorder that might be treated by managing cell stress, a potential therapy for a skin-ear disorder involves blocking cell channels, skin wrinkling may indicate lung aging regardless of smoking, and oxidative stress might contribute to common baldness.

Mechanical trauma like towel drying can cause knotted hair even in straight hair.

Changes in keratin affect skin health and can lead to skin disorders like blistering diseases and psoriasis.

The patient had a severe itchy rash and hair loss in the armpits.

The infant likely has Hay-Wells syndrome and needs genetic testing and heart screening.

Pellagra, caused by niacin deficiency and presenting with photosensitivity, should be considered in patients with relevant symptoms and risk factors.

lncRNAs are important for understanding and treating skin diseases.

A cancer patient's hair became permanently curly after treatment with nivolumab.

New gene variants were found for rare skin and hair disorders, improving understanding and treatment.

KFSD is a rare condition causing scarring hair loss, with no effective treatment known at the time of the report.

The rash resolved after stopping ponatinib.

Trauma can cause fat inflammation and abnormal hair growth.

Severe itching from shingles can cause hair loss due to rubbing.

Acne keloidalis nuchae is a hair loss condition affecting men of African descent, causing scar-like bumps on the scalp and neck.

Skin reactions are a common reason for emergency visits due to drug allergies, with some severe cases needing intensive care.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

cGVHD often severely affects the skin, causing rapid aging and other issues.

Trichotillomania treatment is improving with behavior therapy and new drug approaches, but challenges like stigma and underdiagnosis remain.

The convention discussed various skin conditions, treatments, and the importance of continuous learning in dermatology nursing.

Deleting the CDSN gene causes severe skin and hair problems, leading to death.

Recognizing nail changes helps diagnose and treat non-infectious skin diseases.

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

A 2-year-old girl had a hair disorder not shared by her identical twin.