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A genetic mutation caused severe rickets and alopecia in an Indian patient, but high-dose calcium and phosphate treatment improved their condition.

A specific gene variation is linked to a higher risk of polycystic ovary syndrome in Caucasian women.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

Birth control pills change the activity of certain inflammation and blood clotting genes in women with PCOS.

The PCR technique can identify genetic differences in a wool-related gene among different sheep breeds, which may help improve wool and pelt quality.

Higher GPER-1 levels are linked to more severe and shorter-duration androgenetic alopecia, suggesting GPER-1 as a potential treatment target.

Sensory neuron and Merkel-cell changes in the skin happen independently during normal skin maintenance.

The 1550 nm fractional Er:Glass laser improved hair regrowth in patients with androgenic alopecia, but didn't significantly change collagen type I, skin fibroblasts, or macrophages. More research is needed for optimal results.

Faulty Notch signalling may cause hair follicle changes and inflammation in hidradenitis suppurativa.

A new type of rapid hair loss called ADTA usually gets better on its own within 6 months.

PAI-2 helps in the maturation and protection of hair and nail cells.

The vitamin D receptor can work without its usual activating molecule.

Topical 0.1% tacrolimus significantly improved ear infections in cats.

Urokinase, a type of protein, helps skin cells multiply faster, especially in newborn mice.

A genetic marker linked to a type of hair loss was found in most patients studied.

Frontal Fibrosing Alopecia is a type of hair loss affecting mostly older women, with no agreed best treatment.

Teens with PCOS have a higher risk of type 2 diabetes and need regular glucose checks.

A 15-year-old girl has a skin condition causing blisters on her feet, likely inherited from her family.

Different human traits like skin color and hair type vary between populations due to genetic adaptations to the environment.

Women with Polycystic Ovary Syndrome (PCOS) have lower levels of a substance called DIAPH1 in their blood, which is linked to changes in sugar metabolism and insulin resistance.

Alopecia areata, a type of hair loss, is likely an autoimmune disease with a genetic link, but its exact cause is still unknown.

The SOSTDC1 gene is crucial for determining sheep wool type.

Cholesterol-related compounds can stop hair growth and cause inflammation in a type of scarring hair loss.

Different halogens on progesterone derivatives can either block or mimic male hormone effects, depending on their type and amount.

Alfredo Rebora suggested a new, easier way to classify hair loss in Telogen Effluvium, adding a type possibly related to autoimmune diseases.

Plant-based products can improve hair and skin health without harmful side effects.

In September 2016, there were major advancements and promising clinical trials in stem cell research and regenerative medicine.

The document concludes that individuals with a rare genetic disorder linked to the AEBP1 gene may experience a unique type of hair loss and should be monitored for heart issues.

Lower vitamin D levels are linked to higher CRP levels in people with a type of hair loss called alopecia areata.

The document concludes that Syndromes of Severe Insulin Resistance are rare disorders with limited treatment options.