Search

everythinglearnresearchcommunity

for

Search:↓

Genetics, stress, and health issues can cause early hair greying, which affects self-esteem, and there's no cure, only hair dye.

Alopecia areata involves immune response and gene changes affecting hair loss.

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

Familial factors affect hair loss types in Koreans, with M type in men, L type in women, and paternal factors influencing male hair loss more.

Researchers found a gene mutation responsible for a rare hair loss condition.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

Some congenital hair disorders improve with age and can be managed with treatments like minoxidil, retinoids, supplements, and gentle hair care, but there's no cure.

New genes linked to ichthyosis were found, but there's still no cure; treatment options are improving.

Children's hair loss has many causes and requires careful diagnosis and personalized treatment, including emotional support.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

EDA2R gene linked to hair loss.

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

Smoking and drinking worsened hair loss in men with genetic hair loss, while eating and sleeping habits didn't; genetics played a bigger role than environment in hair loss.

The document concludes that careful evaluation is key to diagnose and treat women with hair loss, with tests for thyroid, iron, and hormones as needed.

Mice are useful for researching human hair loss and testing treatments, despite some differences between species.

The conclusion is that treatments like finasteride and minoxidil can prevent baldness progression and improve hair density, but more research is needed on other therapies.

Certain genetic markers linked to wool quality in Rambouillet sheep were identified, which can guide better breeding choices.

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

Skin issues can indicate immune system problems.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

Genetic defects in testosterone production can cause hormonal and developmental disorders, and more research is needed to understand androgen regulation and develop safer treatments.

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

Various treatments exist for hair loss, but more research is needed for better options.

Four genetic risk spots found for hair loss, with WNT signaling involved and a link to curly hair.

Mutant mice help researchers understand hair growth and related genetic factors.

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

The enzymes Tet2 and Tet3 are important for skin cell development and hair growth.

Men with enlarged prostates often have more severe baldness.