Search

everythinglearnresearchcommunity

for

Search:↓

Genetic variants can affect valproic acid's effectiveness, side effects, and levels in epilepsy treatment.

Afro-textured hair needs personalized care due to its unique genetic traits.

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

Woolly hair is a rare genetic condition with no effective treatments.

Children's hair loss can have various causes, including infections, autoimmune issues, physical stress, nutritional problems, and genetic factors.

Androgenetic alopecia in men is genetic and linked to health issues like obesity and heart disease, with treatments including minoxidil, finasteride, and hair transplants.

Genetic factors could lead to personalized treatments for hair loss.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

Alopecia Areata affects people of all ages worldwide, is likely caused by genetic and environmental factors, and can lead to stress and depression, highlighting the need for treatments that address both physical and mental health.

Genetic research may lead to better ways to predict and treat male-pattern hair loss.

Certain genetic variations in camels affect hair coarseness.

A 12-year-old girl's hair loss was linked to a rare genetic condition called ALX4-related frontonasal dysplasia.

Alopecia areata causes sudden hair loss, has genetic links, and can be managed but not cured.

The guidelines suggest using various treatments, including antidepressants and steroids, for alopecia areata and discuss the condition's genetic and immune aspects.

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

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

Congenital alopecia areata may have genetic links and topical corticosteroids are an effective treatment.

Forensic DNA phenotyping is becoming useful for predicting physical traits in criminal investigations but is limited by ethical concerns and incomplete genetic understanding.

Six genetic conditions are often linked to complete scalp hair loss in children.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

Genetic testing confirmed a rare skin disorder in a young girl, which improved with zinc supplementation.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

Hairlessness in mammals is due to complex genetic changes in both genes and regulatory regions.

The document concludes that the development of certain tumors is influenced by genetic background and that a specific gene modification can lead to tumor regression and reduced growth.

Men can have genetic risks for PCOS-related traits like obesity and diabetes.

Over half of the dog skin disorders discussed have known gene variants, enabling genetic testing for diagnosis and responsible breeding.

Certain gene variations are linked to a higher risk of severe acne, suggesting a genetic influence on the condition.

A girl with a rare genetic condition affecting hair and nails also developed a common type of hair loss, suggesting a possible genetic link.

A genetic change in the FGF5 gene affects hair growth in cashmere goats.