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Exposure to too much androgen before birth might cause polycystic ovary syndrome later in life.

Insulin resistance is linked to high male hormone levels in women, often seen in those with PCOS.

Insulin resistance is linked to PCOS and can lead to other health issues, but treatments like metformin can help manage symptoms.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Certain gene variants may contribute to high androgen levels in women with polycystic ovary syndrome.

Birt–Hogg–Dubé syndrome is a rare genetic condition causing skin lesions, lung cysts, and a higher chance of kidney cancer.

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

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

Foals can have various skin issues, some genetic, immune-related, or due to infections and allergies.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

Genes linked to wool fineness in sheep have been identified.

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

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

Acne is caused by multiple factors including oil production, bacteria, inflammation, and possibly diet and environment.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

The best animal model for studying male-pattern baldness is the stumptailed macaque, not rats or mice.

Insulin resistance is a key factor in polycystic ovary syndrome, but genetics may also contribute.

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

FoxN1 gene is essential for proper thymus structure and preventing hair loss.

The document concludes that careful history and physical exams are crucial for accurately diagnosing polycystic ovary syndrome and distinguishing it from other similar conditions.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

The document concludes that accurate diagnosis of male and female gonadal disorders is crucial for effective treatment and better patient outcomes.

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.

Accurate clinical, histological, and genetic methods are key for understanding and treating hair disorders.

PCOS is a complex condition that affects women's hormonal balance and metabolism, requiring lifestyle changes and medical management.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

PCOS may have evolved as an advantage in past environments with food scarcity.

New treatments targeting the Hedgehog pathway can help treat advanced skin cancer but may have side effects and their effectiveness in early stages is unknown.

The conference concluded with plans for joint research into children's skin conditions and emphasized the importance of collaboration and patient-focused research.

PCOS is a long-term condition that needs more research for better understanding and treatment.