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Researchers found two genes that may explain why some Casertana pigs don't have hair.

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.

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.

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

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.

Chromosomal differences affect how muscle cells respond to testosterone.

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.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

Taking Propecia might lead to the development of cataracts.

Multiple eye conditions were studied, highlighting the importance of various imaging methods for diagnosis, the vision side effects of drugs tamoxifen and Propecia, and the usefulness of optical coherence tomography for diagnosing and monitoring macular and retinal diseases.

S100A3 protein is crucial for hair shaft formation in mice.

Trichoscopy helps accurately diagnose Netherton syndrome, often mistaken for atopic dermatitis.

A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

Keratosis Follicularis Spinulosa Decalvans is a rare genetic disorder causing skin and hair issues, often inherited through the X chromosome.

Female cuckoo color differences are linked to their unique genes and help avoid male harassment.

More research is needed to understand how testosterone is maintained in adult males.

The analysis of a large pilomatricoma revealed five distinct areas with different gene activity related to hair growth and tumor development.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

Certain gene variations might be linked to severe acne in women but not in men.

Rice bran oil extracted by supercritical CO2 is considered non-genotoxic.

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

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

Finasteride reduces Tourette syndrome symptoms, but results may be limited due to potential biases.