Search

everythinglearnresearchcommunity

for

Search:↓

In June 2019, the stem cell research field saw major progress, including new clinical trials, FDA approvals, and industry collaborations.

The meeting highlighted the importance of genetic testing and multidisciplinary approaches in pediatric dermatology.

Genetic mutations can affect female sexual development, requiring personalized medical care.

Skin symptoms are important for diagnosing infections in children.

Two patients with heart issues had successful surgeries and improved symptoms.

An individual's morning or evening preference can predict changes in their body clock gene expression.

The new rodent model successfully mimics non-lean human PCOS symptoms.

Insulin resistance and high male hormone levels are major causes of Polycystic Ovary Syndrome.

Notch signaling disruptions can cause various skin diseases.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

Myoblast transplantation shows promise for treating various muscle and heart conditions.

Serenoa repens is mostly safe but has some risks, especially at high doses or when used with other products for over two weeks.

People with hair loss conditions may also have thyroid disorders, but more research is needed to understand the connection.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

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.

Developing microRNA-based treatments is hard but has potential.

The infant likely has Hay-Wells syndrome and needs genetic testing and heart screening.

The newborn with Klippel-Trénaunay syndrome was healthy but needed regular check-ups for possible complications.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Some skin diseases and their treatments can negatively affect male fertility.

The document concludes that parathyroid diseases have a range of clinical features and outcomes, with some conditions being treatable and others having a high risk of mortality.

Ellis van Creveld syndrome, a rare genetic disorder, can cause unexpected abnormalities in various body organs, requiring thorough patient evaluations.

A patient with a rare hair condition and skin disorder showed hair improvement after treatment.

Covers common skin issues in kids, their diagnosis, treatment, and need for specialist care.

A 19-year-old male with delayed puberty was successfully treated for a condition that prevents normal hormone production.

Turkish pregnant women commonly experienced skin issues like itching and acne, and doctors mainly used topical treatments due to safety concerns during pregnancy.

Cantú syndrome is caused by mutations in the ABCC9 gene.

Lack of sleep in mice leads to prostatitis by reducing certain hormones and activating an inflammatory pathway, which can be temporarily fixed with normal sleep.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.