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The document concludes that various findings in rheumatology offer insights into disease severity, treatment responses, and potential risks in medication, with some limitations due to unspecified participant numbers.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

A unique case showed a rare combination of two types of lichen planus on the face.

Most cutaneous adnexal tumors examined were benign and resembled common skin tumors.

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

A dog had a rare skin tumor called desmoplastic tricholemmoma.

Accurate early diagnosis of Lichen Planopilaris is crucial to prevent permanent hair loss.

New insights into the causes and treatments for the autoimmune hair loss condition Alopecia areata have been made.

Dermoscopy is an effective tool for accurately detecting skin cancers.

Steatocystoma multiplex causes recurring skin cysts and needs early recognition for better management.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Pathologists need better education and collaboration with dermatologists for accurate alopecia diagnosis.

Cutaneous lupus erythematosus is a chronic skin disease that can progress to systemic lupus in some cases and requires treatment to prevent recurrences and scarring.

Trichoscopy helps tell apart Frontal Fibrosing Alopecia and Lichen planopilaris by showing different hair and scalp features.

A cat's poor wound healing was linked to a genetic deletion in the COL5A1 gene.

PAON shows skin patterns due to genetic mosaicism.

Female pattern hair loss is different from male pattern hair loss and has unclear genetic causes.

The document concludes that more research is needed to find effective treatments for Lichen planopilaris and Frontal fibrosing alopecia.

Eruptive vellus hair cysts are rare and often misdiagnosed, requiring biopsy for accurate diagnosis.

Genetic testing is crucial for diagnosing rare hair loss disorders.

Ixekizumab successfully treated a rare hair loss condition, leading to complete hair regrowth.

Dermoscopy helped diagnose a rare skin disease which slightly improved with treatment.

CD18-deficient mice developed psoriasis-like skin disease, useful for studying inflammatory skin disorders.

The conclusion is that there might be a link between certain types of baldness and prostate cancer, which could be due to shared hormonal pathways.

Some small molecule antivirals show promise against COVID-19, but more research is needed to understand and improve them.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Early diagnosis and treatment of nail lichen planus in children can prevent permanent nail damage.

Acne necrotica can be effectively treated with topical cream and antibiotics.

The document concludes that misdiagnosis in skin conditions is common, certain treatments can cause allergic reactions, and some skin symptoms are linked to leukemia, especially in certain Japanese regions.