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Advanced imaging techniques are crucial for accurately diagnosing Monilethrix, a rare hair disorder.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

The 2024 guideline updates recommendations for genetic testing, imaging, and sperm retrieval in male infertility.

Thyroid disease can cause hair loss and treating thyroid problems might help with hair disorders.

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

The document concludes that insulin resistance is key in PCOS development and early treatment is crucial to prevent complications.

The document concludes that the fast-growing direct-to-consumer genetic testing market lacks sufficient regulation, posing risks to consumers due to questionable test quality and accuracy.

Androgens can both increase and decrease hair growth in different parts of the body.

Use minoxidil for hair loss; finasteride and dutasteride for men, dutasteride for women.

Shorter CAG repeats may cause hair and skin issues, while longer ones may link to acne.

Alopecia areata causes hair loss, has no cure, and various treatments exist.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

Male pattern hair loss could hint at androgens affecting COVID-19 severity.

Rhodococcus equi causes severe pneumonia in young foals, and effective vaccines are needed due to foals' weak immune responses.

The article concludes that the wool follicle is a valuable model for studying tissue interactions and has potential for genetic improvements in wool production.

Animals that change color with the seasons mainly do so in response to daylight changes, but climate change is causing camouflage problems that may require evolutionary changes.

Thymus transplantation successfully restored immune function in infants with FOXN1 deficiency.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

Researchers created a fully functional, bioengineered skin system with hair from stem cells that successfully integrated when transplanted into mice.

Hair greying is caused by oxidative stress damaging hair follicles and melanocytes.

Different scaffold patterns improve wound healing and immune response in mouse skin, with aligned patterns being particularly effective.

New findings explain how genetic changes, body clocks, and certain molecules affect tissue response to stress hormones.

Certain gene variants may contribute to high androgen levels in women with polycystic ovary syndrome.

Wnt signaling is important for development and cell regulation but can cause diseases like cancer when not working properly.

Human enzymes can detoxify harmful substances but might also increase their cancer risk.

The document concludes that understanding and treating hair loss requires recognizing its various types and using appropriate diagnostic tools and treatments.

The document concludes that future heart disease research should account for sex-specific differences to improve diagnosis, treatment, and outcomes.

The review suggests thorough evaluation and genetic testing for proper diagnosis and treatment of Chrousos syndrome.

Hair problems can be caused by genetics or the environment, and treatment should focus on the cause and reducing hair damage.

Female pattern hair loss has unclear causes, possibly involving genetics, hormones, and environment, and needs better treatments.