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A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Smoking and certain health conditions like thyroid disease may make palmoplantar pustulosis harder to treat.

Pityriasis rubra pilaris is a rare skin disorder with reddish-orange patches and thickened skin, needing better treatment understanding.

The patient's hair has unique structural differences with alternating bright and dark bands.

PIEZO1 helps keep hair follicle stem cells inactive, affecting hair growth.

PAON shows skin patterns due to genetic mosaicism.

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

Ponatinib can cause a rare skin reaction that resolves with topical treatment and temporary drug discontinuation.

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

A new pain-measuring system using sensors and AI can effectively detect pain in mice, which may help assess pain in humans and develop treatments.

Pigmented papules on the ear can be a rare skin condition called cutaneous amyloidosis, treatable with topical tretinoin.

The hair defect is due to abnormal inner root sheath keratinization.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.

RPGRIP1L helps skin cells stick together by blocking PKCβII, which can prevent skin blistering like in pemphigus.

Targeting the PIEZO1 and MLCK axis may offer a new treatment for hair loss.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Ixekizumab effectively treats generalized pustular psoriasis.

Mice with a mutated Dsg3 gene showed severe symptoms but not the typical blistering of pemphigus vulgaris.

A PIK3CA mutation in Schwann cells causes severe nerve damage and increased glycolysis, but early treatment can help.

Epidermal cysts come from the skin, while pilar cysts come from hair follicles.

Papillon-Lefèvre Syndrome causes early tooth loss and skin issues, needing early dental diagnosis.

PRP patients show varied symptoms and need more research to understand related conditions.

Herpes simplex virus infections should be considered in pemphigus patients to avoid unnecessary changes in treatment.

Cosmetic procedures can trigger pemphigus, an autoimmune disease.

A teenager's hair with alternating white and dark bands, known as Pili annulati, is a genetic condition that is usually harmless and often considered attractive.

A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

Plucked hair can help diagnose pemphigus vulgaris early.

White piedra, a rare fungal infection, was diagnosed in two women in a northern climate.

Two Hispanic women developed Plica neuropathica, a condition causing tangled hair, possibly due to hair damage and various risk factors.