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A gene deletion in DSG4 causes sparse hair in some Pakistani families.

REV7 is crucial for genome stability and cancer treatment, making it a potential target for therapy.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

The revised BASP classification for hair loss is less accurate and harder to use but could still be a viable option.

HDAC4 and HDAC7 are crucial for Th17 cell development and could be targeted to treat inflammatory diseases.

A truncated protein linked to breast cancer may change cell adhesion.

A boy with early puberty and laughing seizures was treated, stopping seizures and slowing puberty.

Growth hormone-releasing hormone (GHRH) boosts hair growth and human scalp hair follicles have their own growth hormone system.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

A woman's hair loss and other symptoms were due to a rare hormone deficiency treatable with steroids.

DS-2325a is safe and well-tolerated, supporting further development for Netherton Syndrome treatment.

7DHC and BM15766 damage hair follicle structure and reduce key gene expression.

The DWLSM provides detailed imaging of hair shafts and follicles with high accuracy.

Combining medication and minimally invasive techniques can effectively manage Marine-Lenhart syndrome.

The gene for Marie Unna hereditary hypotrichosis is located on chromosome 8p21.

A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.

A Saudi individual initially identified as a girl had a genetic disorder affecting gender development.

A gene called HDAC9 might be a new factor in male-pattern baldness.

Hair root sheaths can be used to accurately analyze genetic markers.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

Disrupting the Hars2 gene in mice causes hearing loss due to mitochondrial problems and hair cell damage.

Ptprq has multiple forms that change during inner ear development.

The ZIP7 gene helps control zinc levels in cells by moving zinc from the Golgi apparatus to the cytoplasm.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

A 21-month-old boy has a rare genetic disorder causing sparse hair due to an LSS gene mutation.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

Reduced AhR signaling in HS tunnels leads to persistent inflammation and microbial imbalance.