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The length of the CAG repeat in the androgen receptor gene affects the risk and progression of prostate cancer, BPH, infertility, and undermasculinized genitalia.

LIPH mutations cause woolly hair in some Chinese people.

Woodhouse-Sakati syndrome shows varied symptoms, including hair loss and diabetes, and is common in Qatar due to a specific genetic variant.

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.

CAG repeat numbers in the AR gene likely don't affect male pattern baldness in Korean men.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

Longer CAG and GGN repeats increase alopecia risk, but no significant link to post-finasteride syndrome found.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Tunisian children with hereditary vitamin D-resistant rickets showed improvement with calcium treatment, and new genetic mutations were identified.

Targeting IL-15 may help treat Alopecia Areata.

5% topical minoxidil improves hair density and quality in monilethrix patients.

The N363S gene variant does not cause higher adrenal androgen levels in women with polycystic ovary syndrome.

The HSD3B1 variant increases hair loss risk in overweight women with PCOS.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Olmsted syndrome can be inherited as an autosomal recessive trait due to a rare TRPV3 gene mutation.

Finasteride works better for baldness in people with shorter gene repeats.

Certain genetic variants increase the risk of resistance to hormone therapy in prostate cancer patients.

Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.

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

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

Certain genetic markers can indicate a person's risk of developing prostate cancer.

The genetic variant studied does not affect PCOS symptoms in Kashmiri women.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

Certain gene variations are not a major cause of male infertility in Nigerian men.

Certain genetic variations in the A2M gene are linked to better milk quality in Murrah buffaloes.

A genetic mutation caused severe rickets and alopecia in an Indian patient, but high-dose calcium and phosphate treatment improved their condition.