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The document concludes that certain genetic mutations and dietary factors are involved in acne development, and treatments like isotretinoin and diet changes can help manage it.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

SAHA syndrome is a condition in women involving skin and hair issues, often related to hormonal imbalances, and is treated based on the underlying cause.

PCOS affects women's health by increasing the risk of diabetes, heart disease, and reproductive issues.

The document concludes that careful evaluation is key to diagnose and treat women with hair loss, with tests for thyroid, iron, and hormones as needed.

The most common skin problems in Indian children are infections and eczemas.

The cause of Frontal Fibrosing Alopecia is unclear, diagnosis involves clinical evaluation and various treatments exist, but their effectiveness is uncertain.

Insulin resistance contributes to hormone imbalances in many women with polycystic ovary syndrome.

Drugs targeting the JAK/STAT pathway can improve atopic dermatitis but vary in effectiveness for vitiligo and alopecia areata, with generally mild safety concerns.

CYLD mutations cause a variety of skin tumors with symptoms starting around age 16, and treatments are currently limited.

Early and personalized treatment for hair loss in young people is crucial to prevent permanent damage and should include psychological support.

People who carry the 21-Hydroxylase Deficiency gene are not more likely to have excessive male hormone levels.

Early onset baldness in men may indicate a condition similar to PCOS, linked to heart disease, diabetes, and prostate issues.

Proper control of β-catenin activity is crucial for development and preventing diseases like cancer.

The document concludes that certain mutations may contribute to the inflammation in hidradenitis suppurativa and suggests that targeting TNFα could be a treatment strategy.

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

The conclusion suggests that PCOS may persist due to genetic traits that, while harmful for female fertility, could have provided survival and reproductive benefits to males.

The research suggests that autophagy-related genes might play a role in causing alopecia areata.

Unwanted facial hair significantly impacts over 40% of women's psychological and social well-being, and various treatment options are available.

A rare genetic skin condition usually affecting males was found in a 9-year-old girl.

Effective treatments for spinal and bulbar muscular atrophy are not yet available; more research is needed.

Acne is caused by multiple factors including oil production, bacteria, inflammation, and possibly diet and environment.

A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

Combining plasma rich in growth factors with hair transplant surgery may lead to faster recovery and better outcomes for hair loss treatment.

Four children had unmanageable pale blond hair due to uncombable-hair syndrome.

Various treatments exist for hair loss, but more research is needed for better options.

Found different proteins in balding and non-balding cells, giving insight into hair loss causes.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

New genes linked to ichthyosis were found, but there's still no cure; treatment options are improving.