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

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

Six new genetic regions linked to early hair loss also connect to Parkinson's disease and prostate cancer, possibly leading to new treatments.

Hidradenitis suppurativa is caused by genetic factors, inflammation, bacteria, hormones, and lifestyle factors like obesity and smoking.

Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

The conclusion suggests that PCOS may persist due to genetic traits that, while harmful for female fertility, could have provided survival and reproductive benefits to males.

Blood tests can help understand the genetic differences in people with alopecia areata, including how severe it is and if it's inherited.

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.

Genetic differences within ethnic groups may affect prostate cancer treatment effectiveness.

The document explains the genetic causes and characteristics of inherited hair disorders.

Men with thinner hair from genetic hair loss may be more likely to have an enlarged prostate.

Different human traits like skin color and hair type vary between populations due to genetic adaptations to the environment.

The hypothesis suggests that PCOS may start early in life due to genetic and environmental factors, influencing future reproductive and metabolic problems.

Different types of skin cells have unique genetic markers that affect how likely they are to spread cancer.

Polycystic ovarian shape is a genetic sign of PCOS and its hormonal and metabolic features can be inherited.

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

Researchers found 15 new genetic links to skin traits in Japanese women.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

Two siblings were found to have a genetic condition causing progressive hair loss and woolly hair, which may often be misdiagnosed.

Polycystic Ovary Syndrome likely starts in childhood and may be genetic and influenced by early hormone exposure.

The review suggests thorough evaluation and genetic testing for proper diagnosis and treatment of Chrousos syndrome.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

The new microrhizotron tool effectively observes and measures pepper plant roots non-destructively.

OCT can effectively screen and diagnose various medical conditions non-invasively.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

Acne significantly affects mental health and quality of life, with research suggesting hormonal and genetic factors in its development and emphasizing early treatment to prevent scarring.

Accurate clinical, histological, and genetic methods are key for understanding and treating hair disorders.

Alopecia Areata is an autoimmune disease affecting hair follicles, influenced by genetic and environmental factors, with rodent models being essential for research.

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

Most patients with cutaneous lupus erythematosus in Bangladesh are young women, with chronic forms and photosensitivity being common.