Search

everythinglearnresearchcommunity

for

Search:↓

Genetics, stress, and health issues can cause early hair greying, which affects self-esteem, and there's no cure, only hair dye.

The document explains the genetic causes and characteristics of inherited hair disorders.

Acne is a common skin condition linked to diet, hormones, and genetics, and early treatment can prevent scarring.

Dermatopathology has made significant progress but many skin diseases remain incurable, requiring ongoing research.

Hormonal imbalances are a key cause of missed menstrual periods in women.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

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

Acne is linked to inflammation and insulin resistance, and is associated with various syndromes that require different treatments.

The chapter explains that there are many genetic skin disorders affecting skin cell formation, including both common and rare types.

The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

Hair follicle sampling is a practical method for measuring biomarkers in children with and without Fragile X syndrome.

The document concludes that understanding genetic mutations in the PI3K-AKT-mTOR pathway can lead to better diagnosis and treatment for certain genetic skin disorders.

Hair shaft disorders are diagnosed through examination and history, with general care and some treatments offering improvement.

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.

Genetics and hormones play a role in male and female hair loss, but more research is needed to fully understand it.

Certain genes and X chromosome patterns may significantly contribute to the development of hair loss.

Certain gene variations and irregular X chromosome activity may contribute to hair loss in women who can have children.

Men have worse COVID-19 outcomes than women due to genetic and hormonal differences.

Key genes are crucial for Drosophila wing development and could be insecticide targets.

Monotreme hair structure and protein distribution are similar to other mammals, but their inner root sheath cornifies differently, suggesting a unique evolution from reptile skin.

The conclusion is that young women with excessive hair growth should be quickly tested for hormonal issues and treated to improve their social well-being.

Stem cells regenerate tissues and their behavior varies by environment, suggesting the hematopoietic system model may need revision.

Follistatin and LIN28B together improve the ability of inner ear cells in mice to regenerate into hearing cells.

Scientists made a mouse model of a serious skin cancer by changing skin cells with a virus and a specific gene, which is similar to the disease in humans.

Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.

Chromosomal changes, including those in the WRN gene and rDNA, may significantly contribute to aging.

Chromosomal differences affect how muscle cells respond to testosterone.

Deleting the MAD2L1 gene in mice led to rapid tumor growth despite chromosomal instability.

Anticonvulsant drugs may cause temporary chromosomal abnormalities.