Search

everythinglearnresearchcommunity

for

Search:↓

Reduced androgens linked to kinky hair disorder and hair loss; 5a-reductase inhibitors may help.

Caffeine may help hair growth in hereditary hair loss.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

A 9-year-old Hispanic girl has Uncombable Hair Syndrome, which may improve with age and biotin treatment.

sPLA2-X is crucial for normal hair growth and follicle health.

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

The document reports a unique case of woolly hair with a combination of conditions not previously seen together.

A boy's hair that was frizzy and hard to comb returned to normal after 9 months, possibly due to genetic factors.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

Alopecia X causes hair loss in young plush-coated dogs and can be treated with various therapies, but hair may regrow and then fall out again.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

Botanical extracts and Minoxidil improved hair condition in a boy with a genetic disorder.

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

Low-dose oral minoxidil is safe for treating children's hair disorders.

Trichoscopy is useful for quickly diagnosing different types of hair loss without needing biopsies.

Neurohormones help control skin health and could treat skin disorders.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

Some cosmetics and dermatological drugs can cause allergic reactions and side effects, like skin irritation and systemic issues.

Dermatological conditions are complex and treatments often have mixed results.

The most common skin problems in Indian children are infections and eczemas.

The European Society of Cutaneous Lupus Erythematosus created a questionnaire to standardize patient assessment and improve care for cutaneous lupus.

Some domesticated animals have the same genetic skin diseases as humans, which can help doctors understand human genetic mutations.

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

A new 3D culture system helps grow and study mouse skin stem cells for a long time.

Some skin diseases and their treatments can negatively affect male fertility.

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

Children's hair grows in different types from before birth through puberty, with growth rates and characteristics varying by age, sex, and race.

A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.