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Cannabinoid and steroid-based drugs could be new treatments for Tourette syndrome, but more research is needed to confirm their effectiveness and safety.

Trichotillomania in dementia may be better treated with dopamine blockers like quetiapine than with SSRIs.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

DFMO treatment improves hair growth, muscle tone, and development in Bachmann-Bupp syndrome patients.

All five human steroid 5α-reductase enzymes are found in the endoplasmic reticulum.

Finasteride may help treat autism by reducing inflammation and oxidative stress.

The document suggests a new way to categorize skin and mind disorders into two main groups to reduce confusion.

Choose anti-epileptic drugs carefully for women of childbearing age to avoid risks during pregnancy.

Low vitamin D3 and ferritin levels may cause hair loss in pregnant women.

Schizophrenia risk genes may affect early brain development, contributing to the disease.

Using quantitative traits in genetics can improve understanding and management of skin health and conditions.

A baby with KID syndrome died from infections and organ failure at 18 months old.

Children with autism have lower levels of essential and toxic trace elements in their hair.

New method finds genetic links between Type 2 Diabetes and Prostate Cancer not seen before.

The document concludes that understanding genetic mutations in the PI3K-AKT-mTOR pathway can lead to better diagnosis and treatment for certain genetic skin disorders.

Four new cases of Bachmann-Bupp syndrome suggest potential for targeted treatment.

Key genes and pathways involved in thyroid eye disease were identified, aiding potential treatment and diagnosis.

Researchers identified five new potential targets for leishmaniasis treatment, suggesting repurposing existing drugs could be effective.

New genetic mutations linked to rare skin disorders were found in three newborns.

Epidermal stem cells show promise for treating orthopedic injuries and diseases.

Autism's genetics are linked with early age of puberty and less hair loss, but not with hormone levels or polycystic ovary syndrome.

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.

Certain genes related to sulfur metabolism are more active during the growth phase of Cashmere goat wool, and melatonin might help this process.

Bovine milk-derived exosomes may improve skin, hair, gut, brain, and bone health.

OXTR agonists may promote hair growth and be effective for treating hair loss.

Meis2 is essential for touch sensation and proper nerve connection to touch receptors in certain skin areas of mice.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

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.

Some brain cancer cells avoid immune system detection, and certain treatments could target this to slow their growth; also, certain fat cell precursors help regenerate hair and skin after injury.