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Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

L-PGDS has specific binding sites for its functions and could help in drug delivery system design.

Acne is linked to inflammation and insulin resistance, and is associated with various syndromes that require different treatments.

The document concludes that patient outcomes for Congenital Adrenal Hyperplasia are often not ideal because of poor management and a need for better diagnosis and treatment methods.

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

The meeting highlighted the importance of genetic testing and multidisciplinary approaches in pediatric dermatology.

Genetic mutations can affect female sexual development, requiring personalized medical care.

The document covers various dermatological treatments and conditions.

Gene mutations can cause problems in male genital development.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

UK medical students lack dermatology education, liver biopsy patients with risk factors show more fibrosis, and certain fungi resist drugs due to melanin; genetics may influence female hair loss.

The document suggests a bacteria plays a significant role in acne rosacea and that white hair can regain color after transplant, meriting more research on reversing grey hair.

Insulin resistance is linked to PCOS and can lead to other health issues, but treatments like metformin can help manage symptoms.

The document concludes that Syndromes of Severe Insulin Resistance are rare disorders with limited treatment options.

The workshop highlighted the genetic links and psychological impacts of hair loss and skin disorders.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Researchers found that certain RNA circles in the brain are linked to disease risk, but their exact role in disease is still unknown.

Autism's genetics are linked with early age of puberty and less hair loss, but not with hormone levels or polycystic ovary syndrome.

More precise, personalized therapies are needed for autoimmune diseases.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

The enzyme RDH12 plays a role in vision and retinal disease, with mutations leading to early onset visual loss and blindness, but the exact disease mechanism is unclear and there are no treatments yet.

Melatonin affects gene expression in goat hair follicles, potentially increasing cashmere production.

The rhg mutation in mice affects the Oat gene, causing hair growth issues and other symptoms.

Two siblings with a genetic mutation had a form of rickets that doesn't respond to vitamin D.

Environmental factors can cause mutations in skin proteins, leading to skin disorders.