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The update highlights that non-classic congenital adrenal hyperplasia is common in women with excess male hormones, requires specific hormone tests for diagnosis, and has various treatment options depending on age and symptoms.

The conclusion is that genetic differences affect how the cochlea heals after hair cell loss, which may challenge the creation of hearing loss treatments.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

Higher Lnk protein levels in ovaries may lead to insulin resistance in women with PCOS.

Acne is a chronic skin condition not caused by poor hygiene or diet, and it requires long-term treatment and patient education.

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

Different amounts of daylight affect cashmere growth in goats by changing the activity of certain genes and molecules.

The trial aims to understand how obesity and lifestyle affect circadian rhythms in people with schizophrenia and bipolar disorder.

New treatments and diagnostic methods for various animal skin conditions showed promising results.

Hidradenitis Suppurativa has genetic links, with certain gene mutations more common in patients and a third of cases having a family history.

New method finds genetic links between Type 2 Diabetes and Prostate Cancer not seen before.

The document concludes that both internal stem cell factors and external influences like the environment and hormones affect hair loss and aging, with potential treatments focusing on these areas.

A gene mutation causes woolly hair in a Syrian patient.

The study found that genetic differences related to hair growth and other traits help cashmere goats adapt to high-altitude environments.

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

Deleting Smad4 and PTEN genes in mice causes rapid, invasive stomach cancer.

Deleting Smad4 and PTEN genes in mice causes rapid, invasive forestomach cancer.

SOX4 is crucial for the development of melanoma.

Protease Nexin-1 is found in human hair growth cells and is affected by male hormones.

Hair follicle stem cells prevent melanocyte stem cells from differentiating by controlling retinoic acid levels.

Root hair growth in plants is a complex process controlled by many factors working together.

Apoptosis may contribute to hair loss in androgenetic alopecia.

Targeting CD200 could be a new treatment for rheumatoid arthritis.

Certain immune-related proteins are higher in people with alopecia and their healthy relatives, hinting at a genetic link.

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

Certain microRNAs may protect against hair loss in alopecia areata and could be potential treatment targets.

Low iron levels may be linked to some types of hair loss in women.

Mice with human skin protein K8 had more skin problems and cancer.

Diabetes causes lasting cell dysfunctions, leading to serious complications even after blood sugar is controlled.