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Genetic defects in testosterone production can cause hormonal and developmental disorders, and more research is needed to understand androgen regulation and develop safer treatments.

Myotonic dystrophy should be considered in patients with hair thinning, and genetic counseling is important.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

Certain gene variations may increase the risk and severity of alopecia areata.

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

Genetic analysis of rabbits identified key genes for traits like coat color, body size, and fertility.

Alopecia areata causes sudden hair loss, has genetic links, and can be managed but not cured.

Different people show different symptoms for genetic diseases because of how sensitive their bodies are to small changes in important factors.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Certain gene variations may increase the risk of alopecia, and platelet-rich plasma treatment can improve hair density in those with hair loss; a rare case of facial Becker's nevus was linked to uneven beard growth.

Certain gene variations might increase the risk of a hair loss condition in Koreans.

Treat genetic hair loss early with FDA-approved medications and consider hair transplantation.

Chinese domestic goats have unique genetic traits due to domestication and geographic isolation.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

Certain gene variations in the Vitamin D receptor may increase the risk of chronic hair loss.

Certain gene variations in EGF and EGFR may increase the risk of alopecia areata in Koreans.

Certain genetic variants linked to immune response increase the risk of alopecia areata in Taiwanese people.

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.

Certain gene variations in AKT2 are more common in women with PCOS and are linked to higher levels of specific hormones and symptoms.

New findings explain how genetic changes, body clocks, and certain molecules affect tissue response to stress hormones.

The study suggests certain ACE gene variations are more common in women with PCOS and may be linked to increased insulin resistance.

The research found specific genes that may cause longer hair in Tianzhu White Yak.

Low-coverage sequencing is a cost-effective way to find genetic factors affecting rabbit wool traits.

The conclusion is that certain genetic factors and blood types may affect COVID-19 severity, but changes in ACE2 and TMPRSS2 genes are not clearly linked to it.

Female cuckoo color differences are linked to their unique genes and help avoid male harassment.

A specific genetic deletion in goats affects cashmere yield and thickness.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

PCOS is a genetic disorder affecting women's reproductive health, with treatments focused on symptoms like insulin resistance and fertility.

Nonclassic congenital adrenal hyperplasia is a common genetic disorder that can cause a range of symptoms and requires personalized treatment.