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A person with Turner Syndrome showed severe schizophrenia that didn't respond to treatment and had brain shrinkage.

Conditions affecting sex development show that sexual diversity is a natural part of human variation.

Infertile men are more likely to produce sperm with abnormal chromosome numbers, which can affect pregnancy success and embryo health.

The scraggly mutation causes hair loss and skin defects in mice.

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

Ring Chromosome 11 may be linked to conditions like early puberty, excessive hair growth, hair loss, and type 2 diabetes.

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

Longer GGN repeats in the androgen receptor gene are linked to polycystic ovary syndrome.

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

Men have worse COVID-19 outcomes than women due to genetic and hormonal differences.

Dermatologists give better information on pathology forms, hypersensitivity vasculitis is a common skin issue, misdiagnoses can occur, and various skin conditions are linked to loss of elastin or genetic factors.

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

Society's pressure to have children later in life favors genes that increase the risk of early baldness in male offspring.

A complex X chromosome rearrangement can increase the risk of multiple autoimmune diseases.

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

Men may be more vulnerable to severe COVID-19 due to genetic and hormonal factors, but more research is needed.

The research concluded that selection significantly shaped the genetic variation of the X chromosome, with certain regions affected by past selective events.

A 6-year-old girl with Turner syndrome also had psoriasis, alopecia areata, and trachyonychia.

The 2024 guideline updates recommendations for genetic testing, imaging, and sperm retrieval in male infertility.

Loss of the Y chromosome and UTY gene activity increases cancer risk in men.

Male pattern baldness is mostly inherited, involves many genes, and is linked to other traits like early puberty and strong bones.

Identical twins had different symptoms because one had more cells with an extra chromosome fragment in different tissues.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

Two mouse mutations cause similar hair loss despite different skin changes.

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

Scientists found a gene in mice that causes early hearing loss.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

Acute leukemias with the Philadelphia chromosome may be biphenotypic, and identifying this is important for proper treatment.

Adult mice with CBS deficiency show minimal health issues and normal lifespan despite high homocysteine levels.

The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.