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Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

The CORT, FGF5, and CD36 genes are crucial for the cold weather adaptation of Yanbian cattle.

Skin aging is caused by stem cell damage and can potentially be delayed with treatments like antioxidants and stem cell therapy.

Six new hair loss factors in men not linked to female hair loss.

An 81-year-old man's white hair began to regain its original color while he was treated with lenalidomide, suggesting that graying hair might be reversible.

DNA methylation and long non-coding RNAs are key in controlling hair growth in Cashmere goats.

No link found between new male baldness genes and female hair loss.

Wnt7a protein is crucial for development and tissue maintenance and plays varying roles in diseases and potential treatments.

XIST RNA helps regenerate hair follicles by targeting miR-424 and activating hedgehog signaling.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

The research identified genes that explain why some sheep have curly wool and others have straight wool.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

Certain gene variations increase the risk of alopecia areata in Koreans.

Certain gene variations might be linked to severe acne in women but not in men.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Frontal Fibrosing Alopecia might be an autoimmune disease.

Certain proteins involved in DNA modification may affect the genetic changes in systemic lupus erythematosus and could indicate the disease's activity.

Genetically modified sheep with more β-catenin grew more wool without changing the wool's length or thickness.

A woman with acne and baldness was found to have a rare ovarian condition but successfully had a child through fertility treatment.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

A specific RNA molecule, circCOL1A1, affects the growth and quality of goat hair by interacting with miR-149-5p and influencing cell growth pathways.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

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.

Certain long non-coding RNAs are important for the growth of hair follicles in Inner Mongolian cashmere goats.

The study concluded that changing the culture conditions can cause sika deer skin cells to switch from a flat to a 3D pattern, which is important for creating hair follicles.

Some skin conditions may increase the risk of heart disease, but are not yet included in cardiovascular prevention guidelines.

No clear link between specific gene and hair loss in Mexican brothers.

Nuclear shape and chromatin changes affect gene expression in skin cell differentiation.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.