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Myo-inositol plus α-lactalbumin works better than myo-inositol alone for improving symptoms of PCOS.

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

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

Lipid Accumulation Product and Free Androgens Index are effective for assessing fatty liver disease risk in women with Polycystic Ovary Syndrome.

Baldness is linked to a higher risk of coronary artery disease, but not to its severity.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

L-PGDS has specific binding sites for its functions and could help in drug delivery system design.

Activin A and follistatin control when ear hair cells form in mice.

Activin A promotes ear hair cell development, while follistatin delays it.

Hair follicle stem cells can change their role to ensure proper hair development.

Fetuin A may increase collagen production and promote scarring.

Scientists created a tiny, 3D model of a hair follicle that grows and acts like a real one.

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

The document tests knowledge and decision-making in hematology through multiple-choice questions.

The document provides 70 multiple choice questions to improve haematology skills.

Gene mutations can cause problems in male genital development.

The document concludes that transsexual individuals often experience improved quality of life after transitioning, despite higher risks of psychiatric issues and mortality.

Minoxidil solution and foam both increase hair growth, but the solution works better than the foam.

Androgenetic alopecia is linked to a higher risk of coronary heart disease due to certain genetic factors and high homocysteine levels.

The Wnt/β-catenin pathway is important for body functions and diseases, and targeting it may treat conditions like cancer, but with safety challenges.

Planarian regeneration begins with a specific gene activation caused by injury, essential for healing and tissue regrowth.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

Sensitive skin is often caused by nerve fibers and environmental factors, and can be managed with mild skincare and professional advice.

Understanding how DHT works is important for diagnosing and treating hormone-related disorders.

Regenerative pharmacology, which combines drugs with regenerative medicine, shows promise for repairing damaged body parts and needs more interdisciplinary research.

Mutations in the KRT85 gene cause hair and nail problems.

The mineralocorticoid receptor may play a role in skin and hair health and could be a new target for treating related disorders.

Keratin proteins are essential for keeping the cells in the human colon healthy and stable.

Certain genetic variations are linked to increased androgen levels in PCOS, but more research is needed to understand these connections fully.

Looking at skin can help find and treat serious diseases early.