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The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

Korean Red Ginseng has beneficial components that help with stress, immunity, fatigue, memory, blood flow, and disease protection.

Finasteride effectively treats enlarged prostate and male baldness, improves symptoms of hirsutism in women, but doesn't work for acne, and may delay prostate cancer progression with few side effects.

Formyl-peptide receptor agonists could be new anti-inflammatory drugs.

KAP genes are crucial for hair development and show both shared and unique traits in humans, chimpanzees, and baboons.

Cri-du-chat syndrome can cause skin and oral lesions affecting nutrition and quality of life.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

Understanding how EDC genes are regulated can help develop better drugs for skin diseases.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Hexi cashmere goats' hair growth varies by stage, with Hoxc13 linked to hair activity.

Three siblings with a rare genetic condition had abnormal sexual development and chose different gender identities, needing surgery and therapy.

The research found specific genes and proteins that affect how fast chickens' feathers grow, which is not solely determined by traditional inheritance patterns.

Gene therapy shows promise for improving wound healing, but more research is needed for human use.

Environmental factors like diet and vitamin levels, especially Vitamin D, can affect autoimmune diseases differently, with lifestyle changes potentially improving outcomes.

Neurohormones help control skin health and could treat skin disorders.

New treatments for skin conditions related to the sebaceous gland are being developed based on current research.

Certain HLA class II alleles increase or decrease the risk of alopecia areata.

Certain MC4R gene variants are linked to higher BMI in obese women with PCOS but do not cause PCOS.

The enzyme RDH12 plays a role in vision and retinal disease, with mutations leading to early onset visual loss and blindness, but the exact disease mechanism is unclear and there are no treatments yet.

The research found that male pattern hair loss is mostly genetic and involves hair thinning due to hormonal effects and changes in gene expression.

S100A3 protein is crucial for hair shaft formation in mice.

The document concludes that more research is needed to fully understand the causes of PCOS.

Finasteride reduces Tourette syndrome symptoms, but results may be limited due to potential biases.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

Mutations in the glucocorticoid receptor gene cause reduced sensitivity to glucocorticoids and may lead to poor response to treatment.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in Tourette syndrome patients.

Finasteride may help reduce tic severity in male Tourette syndrome patients.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in patients with Tourette syndrome.