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The conclusion is that genetic changes in the glucocorticoid receptor can lead to conditions affecting stress response, immunity, and metabolism, requiring personalized treatment.

Genetic defects in the glucocorticoid receptor gene can cause conditions with abnormal sensitivity to stress hormones, and other factors may also affect this sensitivity.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

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

A genetic mutation in the LIPH gene causes hair loss and growth defects.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

Understanding genes can help diagnose and treat skin color disorders.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

Certain Egyptian Sabal fruit extracts may help treat anti-androgenic diseases like benign prostatic hyperplasia.

Genetic mutations can affect female sexual development, requiring personalized medical care.

Genetic defects and UV radiation cause skin damage and aging.

Dermatologists give better information on pathology forms, hypersensitivity vasculitis is a common skin issue, misdiagnoses can occur, and various skin conditions are linked to loss of elastin or genetic factors.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

More research is needed to understand the genetic causes of Alopecia areata to develop better treatments.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

Genetic counselors should be culturally skilled and aware of transgender patients' unique health risks and needs.

The conclusion suggests a new way to classify bradykinin-mediated angio-oedema based on different causes and its possible link with urticaria, which could improve diagnosis and treatment.

Certain mutations in the PADI3 gene may increase the risk of developing a type of scarring hair loss common in women of African descent.

There's no significant genetic link between male pattern baldness and COVID-19.

Two sisters with lipoedematous scalp suggest a genetic influence in the condition.

Some domesticated animals have the same genetic skin diseases as humans, which can help doctors understand human genetic mutations.

Food intake, not genetics, affects how the body processes tadalafil and finasteride.

Avoiding smoking, stress, obesity, and poor diet may help reduce hair loss in young Egyptian males.

Understanding keratinization is crucial for treating skin conditions like ichthyoses and psoriasis.

No significant link between male pattern baldness and COVID-19 severity was found.

Autoimmune skin disorders are caused by genetic and environmental factors and are treated with various medications and preventative strategies.

The Rotterdam Study aims to understand disease causes in the elderly and has found new risk factors and genetic influences on various conditions.