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The document concludes that early recognition and treatment of PCOS in adolescents is crucial for managing symptoms and long-term health risks.

Male hormones affect COVID-19 severity and certain drugs targeting these hormones could help reduce the risk.

Siblings with signs of virilization should be tested for non-classical congenital adrenal hyperplasia, which does not affect adult height but may impact fertility and well-being if untreated.

Hidradenitis suppurativa is caused by genetic factors, inflammation, bacteria, hormones, and lifestyle factors like obesity and smoking.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

A 3-month stay in space causes skin thinning, disrupts hair growth, and changes muscle-related genes in mice.

With careful management, people with congenital adrenal hyperplasia can have successful pregnancies and become parents.

The document suggests that targeting the hormone DHT could be a more effective treatment for prostate cancer than targeting testosterone.

People with alopecia areata often have lower levels of vitamin D, zinc, and folate, but more research is needed to understand if supplements can help treat it.

Genetic mutations that disrupt homocysteine breakdown lead to increased damage in mouse hair keratin.

A specific enzyme is essential for proper hair follicle stem cell development and healthy skin.

The workshop highlighted the genetic links and psychological impacts of hair loss and skin disorders.

New treatments for ichthyosis, like protein replacement and gene therapy, show promise and may become standard care.

Feather patterns form through genetic and epigenetic controls, with cells self-organizing into periodic patterns.

ARL15 is important for fat cell development and the release of the hormone adiponectin.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

Eph/ephrin signaling is important for skin cell behavior and could be targeted to treat skin diseases.

Normal levels of DHT can reduce belly fat and increase muscle, but too much can lead to hair loss, prostate issues, and possibly heart disease.

Dlx3 is essential for hair growth and regeneration.

Six genetic conditions are often linked to complete scalp hair loss in children.

Polycystic ovary syndrome, a disorder causing menstrual issues and infertility, can be treated with lifestyle changes, medication, herbal remedies, surgery, and assisted reproductive techniques like artificial insemination and IVF.

Robotic hair transplantation with AI offers more reliable, precise, and efficient hair restoration.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

Existing drug dexamethasone may lower death risk in severe COVID-19 cases; more research needed for other drugs.

Netherton syndrome can cause severe dehydration, infections, and growth issues in infants.

Researchers found genes that control hair color and growth change before the visible coat color changes in snowshoe hares.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

Minoxidil improves blood flow and vessel flexibility, potentially helping with vascular stiffness.

Glutathione helps Arabidopsis roots adapt to low phosphate by regulating a specific growth pathway.

The treatment was ineffective in humans.