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Young women in West Bengal, India, with PCOS often have estrogen resistance, leptin receptor issues, folate deficiency, T2DM, and acanthosis, commonly linked to obesity.

A variant in the ADAM17 gene causes hair loss by increasing protein degradation through TRIM47.

Finasteride dosages should be adjusted based on CYP3A5 genotype and liver function to avoid side effects.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

The ABCG2 gene variant increases the risk of high uric acid and cholesterol, especially in overweight or obese young Mexican males.

Modified β-catenin causes different effects in hair and skin cells, leading to cysts or tumors.

Genetic variants in specific genes cause central centrifugal cicatricial alopecia.

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.

The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.

The research found that the molecule lncRNA-H19 helps hair follicle cells grow by affecting certain cell pathways in cashmere goats.

New LSS gene variants help understand congenital hypotrichosis 14 better.

The rs1128977 gene variant may affect cholesterol and body measurements.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

The CORT, FGF5, and CD36 genes are crucial for the cold weather adaptation of Yanbian cattle.

Mutations in the SNRPE gene cause hereditary hair loss.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

Certain genetic changes in the KAP22-1 gene are linked to better wool quality in Egyptian sheep.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

The conclusion is that androgen receptor gene polymorphism might be a marker for polycystic ovary syndrome, but more research is needed.

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

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

Cantú syndrome may be linked to pituitary adenomas.

The KRTAP22-2 gene in sheep does not significantly affect wool traits.

KRT72 gene helps form hair.

The NUDT15 gene variant causes severe side effects from azathioprine in some Indian patients.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.