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Most hospitalized children with skin issues were boys, with allergic skin diseases like atopic dermatitis being most common, and treatments were usually topical.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Astrotactin proteins are important for brain and skin development and are linked to several neurodevelopmental disorders.

A herbal extract may help treat certain types of hair loss by reducing a specific gene's activity.

Mouse Scube3 affects teeth, tongue, vibrissae, and eye development, but not facial structure or limb growth.

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

Finasteride, often used for hair loss, can potentially cause cataracts.

Recent hair loss research shows some progress, especially in understanding male pattern baldness, but effective treatments for many types of hair loss are still lacking.

The document concludes that hair analysis is not good for assessing nutrition but can detect long-term heavy metal exposure.

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.

Dermatologists diagnose and manage melanoma more effectively than general practitioners.

Ruxolitinib significantly improves multiple autoimmune conditions in APS-1 patients.

Genes related to keratin, skin cell differentiation, and immune functions are key in hedgehog skin and spine development.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

Telogen Effluvium is a common hair loss condition that can be short-term or long-lasting and is often caused by stress, illness, or nutritional issues.

Diagnosing alopecia areata is challenging and requires careful examination and various tests to distinguish it from other hair loss types.

Cats lose fur due to various reasons, including allergies, infections, genetics, hormones, diet, cancer, stress, and some conditions are treatable while others are not.

The study found that certain genes are important for hedgehog skin appendage development and immunity, with spines possibly evolving for protection and infection resistance.

Some skin conditions are associated with other serious diseases, and office microscopy may miss many fungal infections.

Pmg-1 and Pmg-2 are new genes important for skin and mammary gland development.

Alopecia areata is an autoimmune disease causing hair loss, treatable with immune-modulating drugs, and linked to genetics.

BMP signaling controls hair follicle size and cell growth by affecting cell cycle genes.

Cronkhite-Canada syndrome may be more treatable and less severe than previously thought.

A man had a large, rare cyst in his mouth removed after 10 years, which fixed his swallowing and breathing problems.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

Feather patterns form through genetic and epigenetic controls, with cells self-organizing into periodic patterns.

The research identified proteins that change as goat hair follicles begin to form, helping to understand how cashmere grows.

Retinoic acid helps change skin cells and is important for skin development and hair growth.