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Isotretinoin's effects and side effects, like birth defects and depression, might be due to it causing cell death in various cells.

Mice with human skin protein K8 had more skin problems and cancer.

Losing eyelashes or eyebrows can be a sign of many different health problems and needs a careful approach to treat effectively.

Madarosis is the loss of eyelashes and eyebrows due to various health issues and requires thorough examination to diagnose and treat the underlying cause.

Most hospitalized children with skin issues were boys, with allergic skin diseases like atopic dermatitis being most common, and treatments were usually topical.

Researchers found a way to grow cashmere goat hair cells in a lab and discovered that certain conditions improve these cells' growth and characteristics.

A new surgical technique effectively cures acne in most patients.

Keratosis pilaris is a common skin condition causing a bumpy texture, sometimes linked to other diseases, with various treatments available.

The document concludes that each reviewed medical book is useful for its specific area in pediatric care, especially the "Neonatal Formulary" for neonatal drug information.

Combining micro-needling, LED therapy, and growth factors with Finasteride® significantly improves hair growth.

Despite progress in treatment, the exact cause of Alopecia areata is still unknown.

A new method accurately detects bisphenols and parabens in human hair.

Netherton's syndrome is linked to high IgE levels and unique skin and hair symptoms, and may improve with ammonium lactate lotion and allergy management.

The document is a detailed medical reference on skin and genetic disorders.

Ultrasound is a useful, non-invasive tool in dermatology for diagnosing skin conditions and guiding treatments, but it has some limitations.

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

FGF13 gene changes cause excessive hair growth in a rare condition.

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

Dermatopathia pigmentosa reticularis causes skin discoloration, hair loss, and nail problems.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

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

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

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

The document concludes that changes in eyelashes and eyelid skin can indicate various local and systemic diseases.

Autologous cellular micrografts improve hair density and thickness in the short term for androgenetic alopecia.

Melanoma development can be linked to the breakdown of skin's melanin-producing units.

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

A person was born with both a rare hairless condition and a type of birthmark, which is an uncommon combination.

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.

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