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Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

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

The BASP classification is effective for diagnosing pattern hair loss in Indian men and women.

Early onset hair loss in young men is common and linked to family history and alcohol use.

Minoxidil use during pregnancy can cause excessive hair growth and multiple birth defects in the baby.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

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

Familial factors affect hair loss types in Koreans, with M type in men, L type in women, and paternal factors influencing male hair loss more.

Alopecia areata is likely caused by a combination of genetic factors and immune system dysfunction, and may represent different diseases with various causes.

The cause of alopecia areata is likely a mix of genetics, immune system issues, and environmental factors, with more research needed to understand it fully.

Alopecia areata causes hair loss due to an immune attack on hair follicles, influenced by genetics and environment.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

Early hair loss common in Chinese males, linked to family history and smoking; early treatment advised.

Early-onset AGA shows different hair and metabolic characteristics compared to normal-onset AGA.

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

The document concludes that understanding health requires considering evolutionary perspectives on reproductive fitness, and recognizing the complexity of factors like diet, testosterone, and sexual orientation.

Androgenetic alopecia is mainly caused by genetic factors and increased androgen activity, leading to hair follicle miniaturization.

A special gene region controls the re-emergence of a primitive wool type in Merino sheep, improving their wool yield and adaptability.

Hair follicle studies suggest that maintaining telomere length could help treat hair loss and graying, but it's uncertain if mouse results apply to humans.

Female cuckoo color differences are linked to their unique genes and help avoid male harassment.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Prdm1 is necessary for early whisker development in mice but not for other hair, and its absence changes nerve and brain patterns related to whiskers.

Statins may help treat PCOS by lowering androgen levels and improving cholesterol.

Different types of female pattern hair loss have unique characteristics and are associated with various health conditions.

High levels of male hormones in pregnant mice cause heart enlargement and poor heart function in their female babies.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

A girl inherited excessive body hair from her mother and grandmother.

PCOS and related metabolic issues often run in families.

Merkel cells may have roles in sensing magnetic fields, creating fingerprints, Reiki energy healing, passing on environmental information to offspring, and influencing hair shape.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.