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Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

PCOS has a strong genetic basis, but more research is needed to fully understand it.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

No strong genetic link to other skin conditions was found, but some genetic factors may make people more likely to get seborrheic dermatitis.

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

Genetic variants affect minoxidil hair loss treatment success.

PCOS may have evolved as an advantage in past environments with food scarcity.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

FOXN1 gene variants cause low T cells and immune issues from birth.

Haplogroup X found in Altaian population supports Amerindian origin.

IL-4 gene variation may increase the risk of alopecia areata in Turkish people.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.

Certain gene variations and different levels of BDNF and CRH hormones are linked to vitiligo.

Certain gene variants may contribute to high androgen levels in women with polycystic ovary syndrome.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

Some women with PCOS have CYP21 mutations and IRS1 variants, but these genetic factors are not major contributors to PCOS.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

Selecting specific KRTAP26-1 gene variants can improve wool quality in sheep.

Genetic screening is crucial for accurately diagnosing APS-1 due to its varied symptoms.

Certain changes in the SHBG gene may increase the risk of PCOS in Iraqi women.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

Variant G of the KRTAP20-1 gene improves wool curliness in Chinese Tan sheep.

Four new cases of Bachmann-Bupp syndrome suggest potential for targeted treatment.

Chemical exposure may contribute to the rise in atopic diseases and needs more research.

Mexican patients had a lower incidence of skin reactions to drugs and no significant link between these reactions and the TNF2 gene variant.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

A faulty KLHL24 gene leads to hair loss by damaging hair follicle stem cells.