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Hairless gene not strongly linked to baldness.

All-trans retinoic acid causes hair loss by increasing TGF-β2 in hair follicle cells.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

Monilethrix is a genetic hair disorder causing fragile, beaded hair with no effective treatment.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Ovulation disorders are a major cause of infertility and menstrual problems in women.

S5αR inhibitors might help treat schizophrenia and other mental disorders but need more research.

Premature balding in some men may be linked to altered hormones, but it's not the male equivalent to polycystic ovary syndrome or metabolic syndrome.

A specific thyroid hormone resistance mutation may be linked to different types of hair loss.

Hyperandrogenism increases heart disease risk in premenopausal women, but this risk is linked to obesity in postmenopausal women.

A certain gene variation is linked to a higher risk of polycystic ovarian syndrome in South Indian women.

Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

Certain gene variants in estrogen receptors are linked to polycystic ovary syndrome, mainly affecting metabolism, in Tunisian women.

A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.

These specific gene polymorphisms are not linked to Alopecia Areata in Egyptians.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

Patients with one autoimmune disease should be checked for other autoimmune disorders.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

Neurohormones help control skin health and could treat skin disorders.

Topical treatments can deliver active molecules to skin stem cells, potentially helping treat skin and hair disorders, including skin cancers and hair loss.

Lysophosphatidic acid is important for skin health and disease, and could be a target for new skin disorder treatments.

Scalp involvement is common in pemphigus and can lead to hair loss, with the severity of scalp lesions linked to overall disease severity.

Young women in West Bengal, India, with PCOS often have estrogen resistance, leptin receptor issues, folate deficiency, T2DM, and acanthosis, commonly linked to obesity.

Low-dose acitretin helps nail psoriasis, stem cells may treat scarring alopecia, Chinese men have lower baldness rates, lateral foldplasty is good for ingrown toenails, hair diameter helps diagnose female baldness, childhood trauma linked to alopecia areata, certain hair-weaving leads to scalp conditions in African American women, and new methods for hair research and understanding hair and sweat gland development were introduced.

Nonclassic adrenal hyperplasia is a genetic condition that can cause early puberty and fertility problems, treated with specific steroids.

Genes and hormones cause hair loss, with four genes contributing equally.

Premature graying of hair may suggest health issues and currently lacks effective treatments.

Mice are useful for researching human hair loss and testing treatments, despite some differences between species.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.