Search

everythinglearnresearchcommunity

for

Search:↓

New technologies help us better understand how skin microbes affect skin diseases.

New treatments and diagnostic methods for various animal skin conditions showed promising results.

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

Diagnosing hyperandrogenism in women is complex and requires accurate testing methods and consideration of SHBG levels.

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

Thyroid diseases may contribute to autoimmune skin diseases, and more research is needed on their relationship.

The conclusion is that obesity should be managed with a slow, balanced approach to diet and exercise, with medication and surgery as additional options, and education and access to care are important.

Skin problems in COVID-19 patients are rare and may be due to the body's complex immune response or blood clotting issues.

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.

Obesity is linked to various skin conditions and issues, and losing weight can improve these conditions.

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

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

Taurine is important for many body functions and its deficiency can cause health problems.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

Finasteride reduces Tourette syndrome symptoms, but results may be limited due to potential biases.

Finasteride may help reduce symptoms in male Tourette syndrome patients.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in patients with Tourette syndrome.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in Tourette syndrome patients.

Finasteride may help reduce tic severity in male Tourette syndrome patients.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

Genetic screening is crucial for accurately diagnosing APS-1 due to its varied symptoms.

The document concludes that while there are promising methods to control CRISPR/Cas9 gene editing, more research is needed to overcome challenges related to safety and effectiveness for clinical use.

Researchers found a safe and effective way to pick genetically modified skin cells with high growth potential using CD24.

Diagnosing simple-virilizing congenital adrenal hyperplasia can be difficult and requires thorough testing and expert advice.

Obesity affects skin health, causing conditions like acanthosis nigricans and may require different treatment approaches.

Insulin resistance is a key factor in polycystic ovary syndrome, but genetics may also contribute.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.