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The document concludes that eyelash trichomegaly, which is the abnormal growth of eyelashes, can be present from birth, caused by diseases, or result from certain medications.

Personalized treatment with inhibitors, minoxidil, and laser therapy helps hair loss.

Blood tests can help understand the genetic differences in people with alopecia areata, including how severe it is and if it's inherited.

Fine wool sheep have more genes for wool quality, while coarse wool sheep have more for skin and muscle traits.

Platelet-rich plasma may help hair follicle cells grow by affecting certain genes and pathways.

Hormones and genes affect hair growth and male baldness.

The transition from growth to regression in Cashmere goat hair follicles involves changes in expression of genes related to keratin and cell differentiation.

Researchers developed a cost-effective 66 K SNP chip for cashmere goats that is accurate and useful for genetic studies.

Genomic approach finds new possible treatments for hair loss.

Vitamin D and estrogen may help protect heart and kidney health, and maintaining sufficient vitamin D levels could be especially beneficial for African Americans, postmenopausal women, and people with chronic kidney disease.

Researchers found two new genetic variants linked to Alzheimer's disease.

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

DNA can predict physical traits like eye and hair color accurately, especially in Europeans, but predicting other traits and in diverse populations needs more research.

Most adrenal cortex tumors are benign and non-secreting, but proper diagnosis and treatment are important due to the rare possibility of cancer.

Stopping S100A3 activity slows down hair growth in mice.

Male androgenetic alopecia involves hair follicle miniaturization due to DHT, with potential treatments using inhibitors and blockers.

Early-onset baldness is linked to genetics, lifestyle, and can indicate higher risk for heart and metabolic diseases, and affects mental health.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

Chrousos Syndrome is caused by mutations that make the body less sensitive to glucocorticoids, leading to various symptoms and requiring high-dose treatment.

Understanding skin patterns can help us learn about skin diseases and their treatments.

Male and female hair loss have different genetic causes.

New method finds genetic links between Type 2 Diabetes and Prostate Cancer not seen before.

All five human steroid 5α-reductase enzymes are found in the endoplasmic reticulum.

Certain genes related to sulfur metabolism are more active during the growth phase of Cashmere goat wool, and melatonin might help this process.

Genes linked to wool fineness in sheep have been identified.

The Wnt/β-catenin pathway is important for body functions and diseases, and targeting it may treat conditions like cancer, but with safety challenges.

Testosterone is linked to cardiovascular risk factors and stroke, but its exact role is unclear.

Men and women respond differently to drugs for COVID-19, high cholesterol, and diabetes, which suggests a need for personalized treatments.

Sex hormones affect hair growth and loss, and treatments for related hair diseases include various medications, hair transplantation, and light therapy.