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Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

A genetic change in the FGF5 gene affects hair growth in cashmere goats.

Glucocorticoids reduce fat production in liver cells, while androgens increase it in females; manipulating certain enzymes can influence these effects.

Iron deficiency in mothers causes hair loss in their baby mice.

Bioavailable quercetin may help improve aging signs by positively affecting gut health.

Short telomeres may cause symptoms like hair loss and osteoporosis, offering insights into aging.

New methods can better classify curly hair types and lead to improved hair care products.

Women with the NIH type of PCOS have more obesity and higher risk of diabetes and heart disease than those with other types of PCOS.

Removing both KLK5 and KLK7 proteins can prevent death and skin issues in Netherton syndrome.

FGF5 gene mutations cause long hair in domestic cats.

FoxN1 gene is essential for proper thymus structure and preventing hair loss.

Women with PCOS in Sicily show different levels of metabolic problems depending on their PCOS type, with obesity and abnormal lipid profiles being common.

The Foxn1(-/-) nude mouse shows disrupted and expanded skin stem cell areas due to high Lhx2 levels.

Women with different PCOS types have similar fertility treatment results.

PCOS may increase eye pressure and corneal thickness, affecting eye health.

Stem cells are in deep skin layers, while differentiating cells are in shallow layers.

Hedgehog signaling helps keep hair follicle stem cells the same in both young and old human skin.

Brothers of women with PCOS tend to have higher levels of a hormone called DHEAS, indicating a possible genetic link.

Inhibiting AP1 in mice skin causes structural changes and weakens the skin barrier.

Low Vitamin D is common in people with Alopecia Areata, but its impact on the condition needs more research.

miR-29 is a key factor that accelerates aging.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

Low dose finasteride causes only small changes in PSA levels in older men with BPH.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

Long COVID symptoms are common and the new method will help test if remdesivir reduces them.

Men can have genetic risks for PCOS-related traits like obesity and diabetes.

A new mutation in the ST14 gene was found in a patient with ARIH syndrome, showing milder symptoms and no tooth issues.

Manipulating 5α-reductase type 2 can affect liver fat production and glucocorticoid effects.

Loss of a specific protein in skin cells causes symptoms similar to psoriasis.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.