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Lichen planus pigmentosus mainly affects middle-aged women with darker skin, is underreported, and is hard to treat.

The nodule was a benign cutaneous lymphadenoma, not cancer, and was successfully removed.

Canine leishmaniasis is present in Oklahoma, USA.

Congenital adrenal hyperplasia may be linked to adrenal myelolipoma.

Purpura fulminans can signal underlying autoimmune disorders, not just infections.

A genetic mutation in the LIPH gene causes hair loss and growth defects.

A genetic marker linked to a type of hair loss was found in most patients studied.

Immune cells in Hidradenitis suppurativa become more inflammatory and may be important for treatment targets.

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

Activating liver X receptors can reduce fibrosis by stopping certain immune cells from releasing harmful proteins.

A three-year-old girl survived a rare serious infection caused by BCG vaccination, which improved after treatment with a leprosy drug.

Rhupus is a complex syndrome that combines rheumatoid arthritis and lupus, making diagnosis challenging.

A boy with a rare birthmark called verrucous hemangioma needed careful timing for surgery due to its size and depth.

Aggressive immunosuppressive treatment improved a woman's severe heart condition linked to autoimmune disease.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

COVID-19 vaccination may trigger recurrence of cutaneous T-cell lymphoma in some patients.

Lipedematous scalp may have a genetic link and could be associated with psychiatric conditions.

A girl with hereditary chorea, likely Huntington's disease, had her condition worsened by lupus.

Amyloid deposits linked to a type of protein may cause a unique pattern of hair loss by disrupting hair growth cycles.

Lipedematous alopecia causes permanent hair loss due to increased scalp fat.

Ashy dermatosis may be linked to atopy and thyroid disease and can be treated with topical steroids.

Early recognition and management of gastrointestinal tuberculosis in lupus patients are crucial to prevent complications.

ILC1-like cells may contribute to hair loss in alopecia areata and could be new treatment targets.

A rare skin condition was confirmed to be associated with a specific virus in a young girl.

Mycosis fungoides can have unusual symptoms and may be misdiagnosed, but specific cell markers might suggest a lower risk of worsening.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

Lymphocytes, especially CD8+ T cells, play a key role in causing alopecia areata, and targeting them may lead to new treatments.

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

High homocysteine levels in lupus may increase inflammation and cardiovascular risk.

Balancing treatment effectiveness with side effects is crucial for relapsed follicular non-Hodgkin's lymphoma, especially in older patients.