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Certain gene patterns in breast cancer are linked to how active hormone receptors are and could affect patient survival.

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

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

Patients with myotonic dystrophy often have skin problems that suggest early aging and vitamin D issues, and the severity of these problems is linked to their genetic condition and vitamin D levels.

Hair follicle sampling is a practical method for measuring biomarkers in children with and without Fragile X syndrome.

Hair follicle sampling is a feasible method to measure FMRP and FMR1 mRNA levels in children.

Women with myotonic dystrophy might get diseases related to male hormones because their body tissues are extra sensitive to these hormones.

The document concludes that PCOS has a strong genetic component, but more research is needed to fully understand the specific genes involved.

Myotonic dystrophy should be considered in patients with hair thinning, and genetic counseling is important.

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

Certain gene variations are linked to better memory in healthy Chinese women.

The length of CAG repeats in the androgen receptor gene is linked to ovarian reserve but does not affect how the ovaries respond to stimulation.

Different drugs can treat high male hormone levels in women, but they have various effects and some may harm a fetus.

Hormones and their receptors, especially androgens, play a key role in hair growth and disorders like baldness.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

The study suggests that motor neurons created from stem cells of patients with spinal and bulbar muscular atrophy show signs of the disease, including changes in protein levels and cell functions.

Certain gene variations are linked to severe acne in Egyptian patients and could guide treatment choices.

G allele of AR Stul polymorphism linked to higher hair loss risk, especially in white people.

Fewer GGC sequences in the androgen receptor gene improve finasteride treatment for hair loss.

Finasteride side effects in young men may be linked to specific gene variations.

PCOS is a complex condition with major health impacts, needing more research for better diagnosis and treatment.

Most women with excess hair growth have an underlying hormonal issue, often treated with medication and hair removal methods.

Hirsutism in women often indicates a hormonal imbalance and can be managed with a combination of hormonal treatments and hair removal methods.

Human skin makes sexual hormones that affect hair growth, skin health, and healing; too much can cause acne and hair loss, while treatments can manage these conditions.

Low birthweight and rapid weight gain after birth may increase the risk of developing polycystic ovary syndrome.

Certain genes and X chromosome patterns may significantly contribute to the development of hair loss.

Genes and epigenetic changes are important in the development of Polycystic Ovary Syndrome.

Asian hair loss differs from Europeans; consider individual needs and psychological well-being for treatment.

Men with Kennedy disease have less chance of hair loss.