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

Some hair loss disorders are caused by genetic mutations affecting hair growth.

Certain gene variations are linked to a higher risk of severe acne, suggesting a genetic influence on the condition.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

Melasma is now considered a skin aging disorder caused by sun exposure in people with a genetic tendency, which impacts treatment and prevention approaches.

Genetic screening is crucial for accurately diagnosing APS-1 due to its varied symptoms.

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

Passiflora incarnata may help with anxiety but has risks and drug interactions. There's a genetic link between Fragile X Syndrome and Autism Spectrum Disorder. 6.7% of urine cultures showed hospital-acquired urinary tract infections. Children used screens more during COVID-19, causing various health complaints. Autism Spectrum Disorder is often underdiagnosed in females. Dissociative disorders in childhood sexual abuse victims are more common in males. Most pregnant teenagers are not dissatisfied with their body image but worry about weight. Diagnosing tuberculosis after knee surgery is challenging due to non-specific symptoms. Post-COVID-19 syndrome is more common in older, severely affected patients. Psychiatrists should be part of pain management teams due to the psychological aspects of pain.

Scarless healing is complex and influenced by genetics and environment, while better understanding could improve scar treatment.

Hidradenitis Suppurativa is likely an autoinflammatory disease, and better understanding its causes could improve treatments.

Changing the environment around stem cells could help tissue repair, but it's hard to be precise and avoid side effects.

Hair loss risk is influenced by multiple genes.

The document suggests that certain protein deficiencies and scalp blistering in Epidermolysis Bullosa may cause hair loss.

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

Mutations in the desmoplakin gene can cause hair problems and deadly heart disease.

Keratin proteins are crucial for hair structure and strength.

The skin's layers protect, sense, and regulate the body's internal balance, but can be prone to cancer.

Certain gene variants in estrogen receptors are linked to polycystic ovary syndrome, mainly affecting metabolism, in Tunisian women.

Recent selection on immune response genes was identified across seven ethnicities.

Immune cells are essential for early hair and skin development and healing.

The exact cause of frontal fibrosing alopecia is unknown, but it's not likely due to sunscreen.

Hair loss may indicate a higher risk of heart disease and other health issues related to metabolism.

Skin's epithelial stem cells are crucial for repair and maintenance, and understanding them could improve treatments for skin problems.

A 14-year-old boy is the youngest person reported with a rare, benign tumor related to hair follicles, usually found in older people.

Skin issues can indicate immune system problems.

Hidradenitis suppurativa might be a type of autoinflammatory skin disease.

Familial frontal fibrosing alopecia is rare, mostly affects women, and often occurs between sisters or mother-daughter pairs.

Type 2 inflammation helps wound healing by switching immune cells to repair mode.

Early life factors, including a mother's health and environment, can affect the chances of developing polycystic ovary syndrome later in life.