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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.

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.

Scientists have found specific genes linked to different hair loss conditions, which could lead to new treatments.

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

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.

A man with hypoparathyroidism had other health issues that led to a diagnosis of a rare autoimmune disorder, APS-1.

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.

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

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.

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.

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

Lack of certain nutrients may contribute to hair loss and proper diet or supplements could improve it.

AGD1 is important for root hair development in Arabidopsis, working with phosphoinositide signaling and the actin cytoskeleton.

Papillon-Lefèvre Syndrome causes early tooth loss and skin issues, needing early dental diagnosis.

Skin abnormalities can indicate immunodeficiency due to shared origins with the immune system.

Faulty inflammasome activation may lead to autoimmune skin diseases and could be a target for new treatments.

Hair disorders are caused by a complex mix of biology, genetics, hormones, and environmental factors, affecting hair growth and leading to conditions like alopecia.

Family members of North Indian women with PCOS have a high rate of metabolic syndrome.

Skin aging reflects overall body aging and can indicate internal health conditions.

Genetics play a role in acne, but how exactly they contribute is not fully understood.

5α reductase type 2 enzyme mutation and oxidative stress may increase androgenetic alopecia risk in Egyptians.