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The patient with lupus and Degos' disease showed significant improvement with treatment.

The report suggests that hair loss in Cronkhite-Canada syndrome may be caused by alopecia areata incognita, as shown by a patient's improvement with treatment.

Sunlight exposure improved a patient's skin condition, and there may be a link between a certain disease and skin growths; a leukemia treatment caused changes in hair color and growth.

Cronkhite-Canada syndrome is rare, has a poor prognosis, and requires early diagnosis and ongoing treatment.

Early and accurate diagnosis is crucial for managing rare genetic disorders like this localized variant of junctional epidermolysis bullosa.

Dermatologists should recognize diverse discoid lupus signs to avoid misdiagnosis.

The document lists various skin conditions and structures named "corona" that are not related to the coronavirus.

Some cases of folliculotropic mycosis fungoides may progress slowly and not need aggressive treatment.

CD8+ T cells attack hair follicle stem cells, causing scarring and hair loss.

Intracorneal vacuoles are common in parakeratotic skin diseases in dogs, especially with more parakeratosis.

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

Areata-like lupus can mimic alopecia areata but is a form of cutaneous lupus erythematosus.

A new type of pachyonychia congenita may exist, caused by a different keratin mutation.

Tumid lupus erythematosus can cause non-scarring hair loss on the scalp and requires careful diagnosis.

Trichoepithelioma and desmoplastic trichoepithelioma have distinct features that can be identified using reflectance confocal microscopy.

A 23-year-old Syrian woman has two rare hair disorders, and avoiding hair treatments plus using vitamins and minoxidil may help.

A 2-year-old boy with a rare type of lupus causing hair loss improved with oral steroids.

Latanoprost eye drops caused excessive cheek hair growth and eyelash whitening in a woman.

Lichen planopilaris is the most common type of scarring hair loss observed, with a variety of symptoms and tissue changes.

A woman with a rare hair loss condition developed skin cancer in the bald area.

A rare genetic disease caused severe, worsening hair loss from early childhood with poor treatment results.

Buschke-Ollendorff syndrome is a rare genetic disorder causing skin and bone changes, with some cases also showing ADHD or developmental delays.

Certain immune markers may predict chemotherapy response in mesothelioma, and nivolumab is a tolerable and effective treatment for advanced non-small cell lung cancer.

Hand-foot-mouth disease may cause nail loss in children.

Accurate diagnosis and aggressive treatment are crucial to prevent permanent hair loss in cicatricial alopecia.

A rare genetic deletion in the KRT1 gene causes unique skin symptoms in a family.

Vogt–Koyanagi–Harada disease can cause rare hair growth on normally hairless thumb skin.

Early diagnosis and treatment of Lichen Planopilaris are crucial to prevent permanent hair loss.

A 72-year-old man was diagnosed with a rare skin form of Rosai-Dorfman disease after years of misdiagnosis.

Skin lymphoproliferative disorders are hard to diagnose and often linked to systemic diseases, but most have a good prognosis with accurate diagnosis.