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New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

The IRS-2 Asp/Asp genotype may increase the risk of PCOS in Chinese women, especially if they are not obese.

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

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

A new gene mutation causes hereditary coproporphyria with reduced enzyme activity.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

The EDAR gene mutation leads to thinner and more deformed hair shafts.

Nanomaterials can improve wound healing by helping with cell growth, preventing infection, and reducing inflammation.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Niosomes are a promising method for delivering drugs directly to targeted areas in the body.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Oral contraceptive use may increase the risk of frontal fibrosing alopecia in women with a specific CYP1B1 gene variant.

Healthy dogs and cats often carry skin fungi without showing symptoms, which can spread to others.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

Efficient delivery systems are needed for the clinical use of CRISPR-Cas9 gene editing.

New niosomal formulation effectively delivers aminexil through rat skin.

The PON1 192R gene variant is linked to a higher risk of psoriasis and heart disease in Western Mexico.

Swedish men with the E213 A-allele of the androgen receptor have a lower risk of prostate cancer.

The new controlled release PRP therapy shows promise for hair growth in women.

Genetic testing for cancer risk can lead to early and life-saving treatments in people without symptoms.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

Washing can prevent cancer from lubricating oils, extreme body temperatures need more study, Sulfomid is not recognized, no reliable diphtheria carrier treatment except surgery, eyelid injuries should heal before repair, heterophile antibody test is specific for mononucleosis, chlorine inhalations for colds are outdated, and wheat germ is safe.

Liposomes improve the delivery and effectiveness of cosmetic ingredients but face challenges like cost and stability.

DCPA is a chronic leg infection often related to Staphylococcus aureus, affecting mostly young men in India.