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A neglected leprosy treatment led to rare scalp hair loss in an Indian woman, which improved with proper medication.

Oral lichen planus is a chronic disease causing mouth discomfort and sometimes needs immunosuppressive treatment.

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

LiPADI is a useful tool for monitoring the severity and treatment of lichen planus.

Specific immune cells and pathways contribute to hair follicle inflammation and hair loss, suggesting potential treatments for lichen planopilaris.

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

Mutations in the desmoplakin gene can cause hair problems and deadly heart disease.

Researchers identified five new potential targets for leishmaniasis treatment, suggesting repurposing existing drugs could be effective.

SARS-CoV-2 may worsen IPF due to shared genes and pathways, suggesting potential drug targets.

Erosive palmoplantar lichen planus in North-East India mainly affects the feet and often involves nails, with unique inflammatory skin changes.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

Clim proteins are essential for maintaining healthy corneas and hair follicles.

Seven patients were misdiagnosed with discoid lupus instead of lichen planopilaris due to similar symptoms, showing the need for careful diagnosis in scarring hair loss conditions.

Drugs targeting EMT molecules show promise for treating lichen planopilaris.

Women in Australia report different signs of facial aging compared to women in the US, UK, and Canada; men with Lichen planopilaris often have hormonal abnormalities and thyroid disease.

A 30-year-old man with rare skin conditions improved with antibiotics and surgery, hinting at a link to rosacea.

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.

LTBP1 is a key regulator in diseases and a potential target for new treatments.

Different sPLA2 enzymes have unique roles in phospholipid metabolism and biological processes.

Nevus psiloliparus lacks mature hair follicles but keeps other skin structures intact.

Macrophages are more involved in Lichen planopilaris than in Frontal fibrosing alopecia.

Folliculin helps regulate energy and nutrient sensing, impacting Birt–Hogg–Dubé syndrome.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

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.

GLPLS is a rare skin condition with specific hair loss and skin symptoms.

People with cutaneous Lichen Planus are more likely to have Metabolic Syndrome and related conditions like high cholesterol, diabetes, and high blood pressure.

MITF+ melanoma patients are more likely to have multiple melanomas and unique skin patterns.

Basement membrane changes in lichen planopilaris cause scarring and permanent hair loss.