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The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

New gene discoveries have improved diagnosis and treatment for skin and hair disorders, but more research is needed to fully understand them.

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

Blond hair in Solomon Islanders is due to a unique genetic variant, not European ancestry.

Marie-Unna Hereditary Hypotrichosis is a rare genetic condition causing sparse hair growth, requiring specific recognition for proper care.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

Feather patterns form through genetic and epigenetic controls, with cells self-organizing into periodic patterns.

Male pattern hair loss is genetic and influenced by hormones, with treatments like minoxidil and surgery available.

Six new genetic regions linked to early hair loss also connect to Parkinson's disease and prostate cancer, possibly leading to new treatments.

Hidradenitis suppurativa is caused by genetic factors, inflammation, bacteria, hormones, and lifestyle factors like obesity and smoking.

Trichoscopy is a quick and easy way to diagnose most genetic hair problems without invasive methods.

FFA's causes may include environmental triggers and genetic factors.

Genetic variations affecting skin structure play a key role in severe acne.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

The research concluded that selection significantly shaped the genetic variation of the X chromosome, with certain regions affected by past selective events.

The document concludes that managing non-classical congenital adrenal hyperplasia in females requires personalized treatment, genetic counseling, and a team of specialists.

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

Genetic variants linked to ten skin diseases were found, showing both immune and non-immune factors play a role.

A mother and daughter with similar hair loss conditions and identical HLA types suggest a genetic link between the conditions.

Genetic factors affect hair loss, and molecular testing may help predict, diagnose, and treat it.

Myotonic dystrophy should be considered in patients with hair thinning, and genetic counseling is important.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

Over a third of women thought to have non-classical congenital adrenal hyperplasia didn't have it confirmed by genetic tests.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

Different human traits like skin color and hair type vary between populations due to genetic adaptations to the environment.

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

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

Experts discussed hair care, genetic hair defects, hair loss treatments, nail surgery, lupus treatments, skin infections, and cosmetic allergies.

Melanoma's complexity requires personalized treatments due to key genetic mutations and tumor-initiating cells.