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Genetically at-risk healthy people show similar immune issues as those with Pemphigus vulgaris or Alopecia areata.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

PPAR-γ agonists like pioglitazone may help manage lichen planopilaris but don't fully reverse scarring.

The Pemphigus Disease Area Index and Autoimmune Bullous Skin Disorder Intensity Score are the best tools for assessing pemphigus severity.

A man with a type of skin lymphoma had unusual yellowish skin growths despite normal blood lipid levels, and treatment reduced some symptoms but not the growths.

Hair dye ingredient PPD causes cell death and aging in human hair cells by altering microRNA levels.

Topical ruxolitinib quickly improves non-segmental vitiligo.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

Alopecia in VDR knockout mice is due to a defect in hair cycle initiation, not keratinocyte issues.

Substance P may play a role in the inflammation seen in keratosis follicularis spinulosa decalvans.

The woman has a rare skin condition called follicular Dowling-Degos disease, which has limited treatment options.

A 12-year-old boy's hair loss and skin issues improved significantly with medication.

NB-UVB phototherapy is an effective and safe treatment for vitiligo, especially on hands and feet, and can be improved with tacrolimus.

Keratosis Pilaris Atrophicans causes skin scarring and might be treated with a new synthetic retinoid.

Skin cells from people with Epidermolysis Bullosa Simplex have abnormally placed and less active mitochondria.

New treatments and drugs show promise for improving skin pigmentation and regeneration.

Older adults have a wide range of skin conditions, with dry skin being very common and many also experiencing skin growths, itching, and infections.

Two women with darker skin had both frontal hair thinning and skin discoloration.

Poly(ADP-ribose) synthesis is linked to skin cell differentiation.

Polarized microscopy helps identify hair irregularities in genetic disorders.

Acrodermatitis enteropathica is a rare inherited disorder causing skin issues, diarrhea, and hair loss.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

The newborn's skin blisters healed without scarring, leaving some light spots, and stopped forming after four months.

The 3D skin model mimics pemphigus vulgaris and helps test treatments.

Autoimmune myopathy may be linked to hair loss and skin depigmentation.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

Oral zinc gluconate and topical steroids significantly improved a rare scalp condition in three elderly patients.

Some chemicals can permanently or temporarily remove color from skin and hair, which can be distressing and is not well-regulated in cosmetics.

A woman with dermatomyositis showed rare skin symptoms, was treated successfully, and her case suggests checking for cancer in similar patients.

The 308-nm excimer laser is a promising treatment for vitiligo with varying success and mild side effects.