Search

everythinglearnresearchcommunity

for

Search:↓

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.

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.

Trichoscopy is a useful tool for diagnosing hair disorders without pulling out hair.

The study found that hair fragility in Pili annulati may be caused by cavities and damage within the hair shafts.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

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

Hair shaft disorders, often due to genetics or environment, lack specific treatments but can be managed with gentle hair care and may improve with age or topical treatments.

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

Certain genes and nutrients like vitamin D, zinc, and omega fatty acids affect COVID-19 severity and infection risk.

Dermatoscopy helps diagnose hair and scalp disorders in people with Afro-textured hair, but more research is needed for better understanding and treatment.

Childhood ptosis can vary from a minor cosmetic issue to a serious condition and may signal other health problems.

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

Punctate follicular porokeratosis is a skin condition with specific features seen in hair follicles.

Surfactants damage hair, but sealing the cuticle can prevent this.

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

Alopecia areata is a common autoimmune disease affecting about 2% of people, causing significant disability and often associated with mental health issues and other autoimmune conditions.

The conclusion is that androgenetic alopecia and senescent alopecia have unique gene changes, suggesting different causes and potential treatments for these hair loss types.

The Rotterdam Study aims to understand disease causes in the elderly and has found new risk factors and genetic influences on various conditions.

The Rotterdam Study updated its design and objectives in 2012, providing insights into various diseases in the elderly, including skin cancer, bone health, liver disease, neurological and psychiatric conditions, and respiratory issues.

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

Researchers found 63 genes linked to male-pattern baldness, which could help in understanding its biology and developing new treatments.

Nitric Oxide has potential in medicine, especially for infections and heart treatments, but its short life and delivery challenges limit its use.

Creating stronger blockers for skin enzymes might lead to better treatment for conditions like acne and excessive hair growth.

Polycystic Ovary Syndrome is linked to higher risk of hypertension and heart disease.

Understanding how acne develops in different diseases could lead to new treatments.

Autism's genetics are linked with early age of puberty and less hair loss, but not with hormone levels or polycystic ovary syndrome.

Hormonal treatment is effective for women with acne not helped by usual treatments, especially if they have hormonal imbalances.

The research suggests that Tourette syndrome is linked to both brain signaling and immune system pathways.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

Acne is a chronic disease linked to various systemic conditions and has significant psychological and social effects.