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Improper use of ceramic flat irons can cause severe hair damage.

Dermoscopy quickly and accurately diagnosed a rare hair disorder in a 12-year-old girl.

The document concludes that accurate diagnosis of alopecia in children relies on thorough examination and history, and while treatments exist, none can alter the course of alopecia areata, which can significantly affect a child's psychological well-being.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Trichoscopy is a quick, accurate, and non-invasive method to diagnose and treat non-scarring hair loss.

Mice without the vitamin D receptor have bone issues and other health problems, suggesting vitamin D is important for preventing various diseases in humans.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

Sostdc1 controls the size and number of hair and mammary gland structures.

A disease causing skin issues in young adult German short-haired pointers is hereditary, with most affected dogs not responding to treatment.

Skin problems are common in lupus, important for diagnosis, and can be triggered by sunlight.

sPLA2-IIE is crucial for normal hair follicle structure and skin health.

Genetic changes in mice help understand skin and hair disorders, aiding treatment development for acne and hair loss.

The document concludes that proper diagnosis and tailored long-term treatment can effectively manage androgenic disorders in women, improving patient care outcomes.

The vitamin D receptor can act without its usual activating molecule, affecting hair growth and skin cancer, but its full range of actions is not well understood.

Fox genes are important for hair growth and development in cashmere goats.

Patterned hair loss in women is linked to hormonal imbalances and biochemical changes, and should be evaluated for underlying health issues.

Some antiseizure medications can cause reversible hair loss, with valproate, lamotrigine, and carbamazepine being the most common.

A rare hair follicle disorder can cause itchy, bluish-black bumps on the body.

Topical finasteride might be a good alternative for hair loss treatment with fewer side effects, but more research is needed.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Alopecia areata is a chronic condition causing hair loss, with new treatments targeting the immune system showing promise.

Different types of persistent hair loss after chemotherapy respond differently to treatments.

Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.

The conclusion is that treatments for Telogen Effluvium exist, but standard treatment guidelines are needed.

Two mutations in KRT74 and EDAR genes cause sheep to have finer wool.

A mouse gene mutation increases the risk of skin cancer.

Dermoscopy and trichoscopy are useful for diagnosing skin signs in Dermatomyositis.

Skin cysts might help advance stem cell treatments to repair skin.

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.

An elderly woman with cancer improved after treatment for a rare skin condition with coiled hairs.