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Recent findings suggest that genetic factors, immune system issues, and skin cell defects might contribute to the development of hidradenitis suppurativa.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

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

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

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

A new genetic mutation linked to Hutchinson-Gilford progeria syndrome was found in China.

A rare genetic disease caused severe, worsening hair loss from early childhood with poor treatment results.

AGA is a genetic, hormonal hair loss treated with finasteride, minoxidil, and supplements, but new compounds are being developed.

Scientists found new genetic areas that affect how rice root hairs grow and develop.

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

The document explains the genetic causes and characteristics of inherited hair disorders.

Some people have a genetic variation that makes them less effective at breaking down drugs.

Psoriasis is a common, genetically influenced skin disease worsened by stress and lifestyle, but targeted treatments are promising.

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.

Two specific genetic markers increase the risk of hair loss in Asian populations.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

Early diagnosis and genetic evaluation of ADULT syndrome are crucial to reduce stress and medical costs.

Monilethrix is a genetic disorder causing brittle hair, diagnosed using tricoscopy.

A rare genetic mutation caused unusual skin symptoms in a man with Blau syndrome.

Some human genetic markers work for genetic studies in pig-tailed and stump-tailed macaques, which can help in their conservation.

A new genetic model may improve treatment and diagnosis for certain inherited skin diseases.

Combining minoxidil and plant extracts improved hair growth in a boy with a rare genetic disorder.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requiring high doses of calcium and vitamin D for treatment.

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

The dataset includes detailed genetic information from mouse skin cells before and after injury.

The dataset includes detailed genetic information from mouse skin cells before and after injury.

A higher genetic risk score increases the chance of getting benign prostatic hyperplasia and affects treatment outcomes in Han Chinese men.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.