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The dataset includes detailed genetic information from mouse skin cells before and after injury.

The dataset includes detailed genetic information from mouse skin cells before and after injury.

Puberty involves complex hormonal changes, varies by gender and ethnicity, and requires careful monitoring for abnormalities.

The girl's unexpected pubic hair growth led to a diagnosis different from complete androgen insensitivity syndrome.

FGF13 gene changes cause excessive hair growth in a rare condition.

Hair loss in certain mice is linked to changes in keratin-related genes.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

The mouse hairy ears mutation causes longer ear hair due to changes in gene expression.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Different people show different symptoms for genetic diseases because of how sensitive their bodies are to small changes in important factors.

The document concludes that Cutaneous Lupus Erythematosus has different forms, is influenced by genetic and environmental factors, and can be treated with various medications, but more targeted therapies are needed.

Genetic risk for PCOS can affect children's growth, metabolism, and development from early life into adulthood.

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

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

Certain immune cells are linked to non-scarring hair loss, suggesting potential for immune-targeted treatments.

Premature aging increases the risk of immune problems and autoimmune diseases.

An 11-year-old child with total hair loss may have a genetic autoimmune disease, and the outlook for hair regrowth is not good.

Trichoscopy is a useful tool for examining and monitoring hair and scalp conditions.

Retinoic acid affects skin and hair health by working with specific receptors, and its absence can lead to hair loss and skin changes.

Insulin resistance and obesity are key factors in the development and worsening of polycystic ovary syndrome, and lifestyle changes are important for managing it.

Stress can trigger or worsen alopecia areata.

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

Activating β-catenin in mammary cells leads to changes that cause early-stage abnormal growths similar to skin structures.

Adult female acne is a complex condition that can worsen with menopause, requiring holistic treatment and tailored skincare at different life stages.

PCOS may start before birth, involves metabolic issues, and can be treated with drugs like metformin and lifestyle changes.

Alopecia areata is unpredictable, with limited treatment effectiveness, especially in severe cases.

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

Hair problems can be caused by genetics or the environment, and treatment should focus on the cause and reducing hair damage.

Buschke-Ollendorff syndrome is a rare genetic disorder causing skin and bone changes, with some cases also showing ADHD or developmental delays.

The document describes previously unreported unique skin changes in a rare genetic disorder called Hereditary mucoepithelial dysplasia.