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Five new mutations in the androgen receptor gene were found, helping to understand androgen insensitivity syndrome better.

New insights into the causes and treatments for the autoimmune hair loss condition Alopecia areata have been made.

The Rotterdam Study updated its design and objectives in 2012, providing insights into various diseases in the elderly, including skin cancer, bone health, liver disease, neurological and psychiatric conditions, and respiratory issues.

In 2017, pediatric dermatology advanced with new treatments and insights into various skin conditions in children.

Genes play a significant role in male-pattern baldness, and understanding them could lead to new treatments and insights into related health issues.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

Six new genetic regions linked to early hair loss also connect to Parkinson's disease and prostate cancer, possibly leading to new treatments.

Mutant mice help researchers understand hair growth and related genetic factors.

Genetic differences between young and old Tan sheep explain why their fleece changes from curly to straight as they age.

Genetic defects in androgen production are linked to male developmental disorders and are improving treatment understanding.

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

Genetic changes in mice help understand skin and hair disorders, aiding treatment development for acne and hair loss.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

Genetic mutations that disrupt homocysteine breakdown lead to increased damage in mouse hair keratin.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

Genetic screening can help diagnose and manage infertility in Slovenian couples.

Hairlessness in mammals is due to complex genetic changes in both genes and regulatory regions.

The project aimed to understand how genetic test results affect patients' actions and feelings in dermatology.

Marie-Unna Hereditary Hypotrichosis is a rare genetic condition causing sparse hair growth, requiring specific recognition for proper care.

Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.

The conclusion is that genetic differences affect how the cochlea heals after hair cell loss, which may challenge the creation of hearing loss treatments.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

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

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

Studying rare genetic disorders can help us understand and treat common diseases better.

Wild African goats have genetic adaptations for surviving harsh desert conditions.

The workshop highlighted the genetic links and psychological impacts of hair loss and skin disorders.

Behçet's Disease may be caused by genetic and environmental factors leading to abnormal immune responses, and stress management and new treatments could improve patient outcomes.

Fibrodysplasia ossificans progressiva is a rare genetic disorder that causes extra bone growth and symptoms of premature aging.