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Finasteride increases hair count and improves hair growth with low risk of side effects.

Current treatments for androgenetic alopecia manage symptoms but don't cure it, and it affects social and psychological well-being.

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

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

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

The document recommends all three dermatology books for a library, noting their detailed content but also suggesting improvements in clarity and consistency.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

Environmental factors and chemicals might affect hormone balance and contribute to common hair loss.

Frizzled receptors are essential for various body development processes and maintaining certain body functions.

The UD-PrOZA program successfully diagnosed 18% of adult patients with rare diseases, often using genetic testing.

Nanomaterials can improve hair care products and treatments, including hair loss and alopecia, by enhancing stability and safety, and allowing controlled release of compounds, but their safety in cosmetics needs more understanding.

New DNA analysis and machine learning are advancing forensic science, improving accuracy and expanding into non-human applications.

Body hairs can be used in forensic science and toxicology like scalp hair.

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.

Children with Parry Romberg Syndrome had successful facial fat-grafting surgeries after disease stabilization with no complications.

ICL is a condition with low CD4+ T cells like AIDS but not caused by HIV, and normal CD4+ T cell counts may vary between men and women.

Tailor treatments for vitiligo to patient needs for best results.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

Vitiligo is a skin condition causing white spots, more common in women, often starts before age 20, and can affect mental health.

The document concludes that early diagnosis and treatment of Congenital Adrenal Hyperplasia are crucial for preventing serious health issues and improving patient outcomes.

CYLD mutations cause a variety of skin tumors with symptoms starting around age 16, and treatments are currently limited.

Most hair loss in children is caused by a few common conditions, and it's important to diagnose these properly and support the child's mental health.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

The document says menstruation is important for women's health, discusses menstrual disorders, and suggests personalized treatment options.

Lack of cystatin M/E causes thin hair and dry skin.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

Terbinafine can cause hair loss.

Biotin supplements are unnecessary for most people but may help with certain conditions like biotin deficiency, brittle nails, and some hair loss.

No clear link between specific gene and hair loss in Mexican brothers.