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

The document concludes that secondary syphilis cases are increasing and often misdiagnosed, pityriasis rubra pilaris can be distinguished from psoriasis by skin cell features, and different skin layers produce specific components during skin repair.

Hidradenitis suppurativa might be a type of autoinflammatory skin disease.

The girl's itchy armpit and pubic lesions didn't improve with antifungal cream.

Skin cells and immune cells change in a skin condition called hidradenitis suppurativa, and a certain treatment can improve these changes.

A PKP1 gene mutation causes skin fragility and hair loss in Chesapeake Bay retriever puppies.

A girl with a rare skin condition called Keratosis Follicularis Spinulosa Decalvans showed no significant improvement with treatment.

The study found that hair fragility in Pili annulati may be caused by cavities and damage within the hair shafts.

A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.

Plica neuropathica can occur with diffuse alopecia and should be considered in diagnosis.

Keratins are crucial for tissue strength, and mutations in keratin genes can lead to various diseases, highlighting the need for targeted therapies.

Pseudopelade of Brocq is a unique hair loss condition, but its cause and development are still not fully understood.

Avoiding friction and using topical treatments can significantly improve rough skin caused by repeated rubbing.

Prurigo pigmentosa mainly affects middle-aged White and Asian women, often linked to a ketogenic diet, and is best treated with oral antibiotics.

Technique effectively treats deformities, achieves re-pigmentation, and releases scar contractures.

Unilateral keratosis follicularis squamosa may be a new subtype, successfully treated with asiaticoside ointment.

Correct diagnosis and treatment of lupus vasculitis improved the woman's severe symptoms.

A woman with Degos disease managed her condition for nine years with medications and had two healthy pregnancies, while a separate finding suggests a possible link between female pattern hair loss and high blood pressure.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

Myotonic dystrophy may be classified as a segmental progeroid disorder.

Lower 2D:4D finger ratios in HS patients suggest prenatal hormone influence on the disease.

Some medications for inflammation can cause a condition with scalp rashes and hair loss, often linked to Crohn's disease, and may require treatment changes to prevent permanent hair loss.

Photodynamic therapy may not work for erythroplasia of Queyrat and could lead to invasive squamous cell carcinoma.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Catatonia can be a rare sign of lupus, needing careful diagnosis and treatment.

Erosive pustular dermatosis in elderly people may be linked to aging immune systems and skin damage.

Most Recessive Dystrophic Epidermolysis Bullosa patients with a specific mutation likely have Sephardic ancestry from about 500 years ago.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

Myhre syndrome symptoms worsen over time, with specific genetic variants affecting severity.