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Boreal caribou in northeastern British Columbia have significant health issues, including infections, tick infestations, and mineral deficiencies.

Certain natural and synthetic compounds may help treat inflammatory skin diseases by targeting a specific signaling pathway.

Male mice are more susceptible to autism-like changes from valproic acid than female mice.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Quercetin may help improve symptoms of polycystic ovary syndrome.

COVID-19 can cause various skin issues in children, mostly not severe, with chilblain-like lesions being common, especially in adolescents.

Regulatory T cells help heal skin and grow hair, and their absence can lead to healing issues and hair loss.

Certain skin proteins can form anchoring structures without the protein AMACO.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

Obesity leads to physical, metabolic, reproductive issues, higher healthcare costs, and mental health problems.

Lipedema is a painful fat disorder in women that's hard to treat, often worsens with hormonal changes, and requires symptom-focused therapies.

Environmental factors can cause mutations in skin proteins, leading to skin disorders.

The document concludes that more research is needed to reduce frequent hospital visits, addiction medicine education improves with specific training, early breast cancer surgery findings are emerging, nipple smears are not very accurate, surgery for older melanoma patients doesn't extend life, a genetic condition in infants can often be treated with one drug, doctors are inconsistent with blood clot medication, a certain gene may protect against cell damage, muscle gene overexpression affects many other genes, and some mitochondrial genes are less active in mice with tumors.

Cirrhosis affects quality of life with various symptoms, requiring a holistic, multidisciplinary approach for management.

Interventional embolization is effective for treating scalp arteriovenous fistula but can cause complications like swelling and hair loss.

Decursin shows promise for treating cancer, neuroprotection, inflammation, and hair loss.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

Men with androgenetic alopecia, or hair loss, often have abnormal blood flow in their small blood vessels, which might be linked to inflammation and stress.

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

Sirolimus and propranolol may reduce abnormal cell growth and improve lymphatic malformations in children.

Higher serum ferritin levels than currently used might be needed to rule out iron deficiency in women with hair loss.

Minoxidil use during pregnancy can cause excessive hair growth and multiple birth defects in the baby.

Toxic Epidermal Necrolysis is a rare, serious skin condition that can affect anyone, is more common in women, and may be linked to genetics, with a 20% mortality rate mainly due to sepsis.

Gamma-rays exposure during the resting phase of hair growth can damage hair regeneration and color in mice.

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

A mutation in mice causes hair loss and immune problems.

Nevus comedonicus is a rare skin condition with grouped open pores, sometimes linked to other body issues.

Society's view of "freaks" has shifted from natural deformities to extreme plastic surgery, reflecting changing beauty standards and pressures.

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