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New genetic locations explain much of hair color variation in Europeans.

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.

Male and female skin differ due to hormones, affecting conditions like hair loss, acne, and skin cancer, and suggesting a need for gender-specific treatments.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

Group a wide range of chemicals, not just phthalates, for assessing risks to male reproductive health.

The document concludes that managing female hyperandrogenism requires a combination of identifying the cause, lifestyle changes, medication, and cosmetic treatments.

Mast cells play a significant role in hair loss conditions like male pattern hair loss and alopecia areata.

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

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

Sex hormones like estrogen and testosterone may affect COVID-19 severity differently in men and women, potentially influencing prevention and treatment strategies.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

Most hair follicle stem cells do not protect their DNA by dividing it unevenly.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

Hair loss gene found on chromosome 3q26.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

A gene called HDAC9 might be a new factor in male-pattern baldness.

The gene for slick hair in Senepol cattle is located on chromosome 20 and may involve the SRD5A2 gene.

The document concludes that the human keratin gene cluster is complex, with a need for updated naming to reflect over 50 functional genes important for hair and skin biology.

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

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

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.

A special gene region controls the re-emergence of a primitive wool type in Merino sheep, improving their wool yield and adaptability.

Pallister-Killian Syndrome is a complex genetic disorder requiring coordinated care and genetic counseling.

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

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

Chromosomal differences affect how muscle cells respond to testosterone.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

Cicatricial alopecia, a permanent hair loss condition, is mainly caused by damage to specific hair follicle stem cells and abnormal immune responses, with gene regulator PPAR-y and lipid metabolism disorders playing significant roles.

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.