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Certain gene variations and irregular X chromosome activity may contribute to hair loss in women who can have children.

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

The Naked (N) trait in mice is linked to lower glycine and tyrosine in hair proteins.

Early balding in men is linked to metabolic syndrome, so screening is important for prevention.

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

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

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

Longer CAG repeat lengths in the androgen receptor gene are linked to higher testosterone levels in women with PCOS.

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.

The study suggests that a specific gene variation and higher gene activity are linked to increased baldness in Egyptian men.

Two new mutations in the AR gene linked to severe androgen insensitivity were found.

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

Genetic data can predict male-pattern baldness with moderate accuracy, especially for early-onset cases in some European men.

The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

New genetic mutations linked to rare skin disorders were found in three newborns.

EDA signaling is linked to skin disorders, various cancers, and liver disease.

Keratosis pilaris is often linked to genetic mutations and causes skin and hair abnormalities, regardless of those mutations.

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

Long-term use of Risperidone may be linked to a serious skin condition in bipolar patients, affecting their overall well-being.

Some women with PCOS have rare genetic variants linked to the condition.

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

Children's hair loss can be caused by many factors, including autoimmune diseases, emotional stress, genetics, and infections, with treatment and prognosis varying.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

The document concludes that more research is needed to better understand and treat primary cicatricial alopecias, and suggests a possible reclassification based on molecular pathways.

Mice studies show that Protein Phosphatase 2A is crucial for cell growth, development, and disease prevention.

TNF family proteins are crucial for the development of skin features like hair, teeth, and mammary glands.

Assessing newborn scalp hair can reveal important health information.

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