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Isotretinoin was not effective in treating facial lichen planopilaris.

Athletes can experience various skin issues, which can be treated and prevented with appropriate care and protective measures.

Metformin may improve acanthosis nigricans by reducing insulin resistance.

Improved nutrition quickly healed the patient's skin lesions.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

A pregnant woman's skin condition improved after giving birth, possibly due to high estrogen levels during pregnancy.

Atopic dermatitis may have genetic causes and can be treated with pharmacologic methods, glycerin creams, and controlling Staphylococcus aureus colonization.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

Asian patients with Frontal Fibrosing Alopecia often lose eyebrow hair and respond well to combined antiandrogen or antimalarial and topical treatments.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

No effective treatment exists to stimulate hair growth in atrichia with papular lesions.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

Multiple eye conditions were studied, highlighting the importance of various imaging methods for diagnosis, the vision side effects of drugs tamoxifen and Propecia, and the usefulness of optical coherence tomography for diagnosing and monitoring macular and retinal diseases.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

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

A boy developed a rare skin condition after recovering from a severe skin reaction, and it improved with lotion treatment.

A rare skin condition causes red and dark patches on the face and limbs.

Perifollicular elastolysis is poorly understood, with limited treatment options and inconsistent results.

Follicular porokeratosis may be linked to diabetes and can lead to hair loss.

Sarcoidosis is more common and severe in Black patients than in Caucasians, requiring early diagnosis and treatment.

Dermoscopy helps diagnose rare GLPLS in males.

Dermoscopy helps diagnose folliculotropic mycosis fungoides by identifying specific skin patterns.

Pulsed infrared laser can effectively reduce symptoms of pseudofolliculitis barbae.

Permanent makeup can cause delayed allergic reactions, but they can be managed with proper treatment.

This rare genetic disorder causes permanent hair loss and skin bumps from birth.

Skin symptoms can indicate endocrine disorders and have various treatments.

Folliculotropic mycosis fungoides can occur in children and is diagnosed with specific tests, but often stays in early stages with treatment.

Lichen planus is a skin condition that can resolve on its own, is linked to hepatitis C, and increases the risk of skin cancer.

Looking at skin can help find and treat serious diseases early.