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

Monilethrix has no effective treatment, but avoiding hair trauma helps manage it.

An Australian with rare hair loss and eye conditions had a gene linked to both, not seen together before.

Two specific genetic markers increase the risk of hair loss in Asian populations.

Frontal Fibrosing Alopecia is a hair loss condition mainly affecting postmenopausal women, with unclear causes and various clinical patterns.

A teenager's hair with alternating white and dark bands, known as Pili annulati, is a genetic condition that is usually harmless and often considered attractive.

A girl inherited excessive body hair from her mother and grandmother.

Environmental factors like smoking, UV exposure, and poor diet contribute to hair loss and graying, and lifestyle changes can help manage it.

Certain genes are linked to the risk of developing Alopecia Areata.

A special gene region controls the re-emergence of a primitive wool type in Merino sheep, improving their wool yield and adaptability.

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

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

Hox genes control hair follicle stem cell regeneration in different body regions.

Male pattern baldness is partly caused by specific genes, but most genetic factors are still unknown.

People with Down syndrome are more likely to experience hair loss, and using dermoscopy can help diagnose it.

A defective gene causes hair loss and taste insensitivity in BTBR mice.

The document concludes that current treatments for androgenic alopecia are not fully effective, but new therapies like botulinum toxin and PRP show promise, and future gene therapy could be beneficial.

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

The meeting discussed various skin conditions, treatments, and unusual cases, highlighting the effectiveness of tetracycline in treating rosacea.

Four genetic risk areas related to male-pattern baldness were identified, with WNT signaling playing a role in its development.

Androgenetic alopecia is mainly caused by genetic factors and increased androgen activity, leading to hair follicle miniaturization.

Longer GGN repeats in the androgen receptor gene are linked to polycystic ovary syndrome.

DSDs are birth conditions causing unusual sex development, managed with personalized care and sometimes surgery, but still lack a standard treatment approach.

Men may be more vulnerable to severe COVID-19 due to genetic and hormonal factors, but more research is needed.

The research found that genetic factors for male pattern baldness in African men differ significantly from those in Europeans.

Conditions affecting sex development show that sexual diversity is a natural part of human variation.

Dermatologists give better information on pathology forms, hypersensitivity vasculitis is a common skin issue, misdiagnoses can occur, and various skin conditions are linked to loss of elastin or genetic factors.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

Society's pressure to have children later in life favors genes that increase the risk of early baldness in male offspring.