Search

everythingexperts & clinicslearnresearchcommunity

for

Search:↓

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

Family history affects onset and severity of androgenic alopecia, but treatment success depends more on therapy duration.

Generalized vitiligo in Chinese patients is linked to other autoimmune diseases, especially in familial cases.

AR/EDA2R gene linked to early-onset female hair loss, but 20p11 gene not involved.

Alopecia areata often starts before age 20, is more common in women, and may have a genetic link with other autoimmune diseases.

Age, race, family history, and certain genetic factors increase prostate cancer risk.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

Certain types of alopecia areata are linked to allergies, autoimmune diseases, and family history.

Certain genetic markers may increase or decrease prostate cancer risk.

Precocious puberty can signal familial adenomatous polyposis.

UV photography can help identify people at higher risk for skin cancer, and male pattern baldness at age 45 is linked to a higher risk of certain skin cancers.

Male pattern baldness may predict prostate cancer risk.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

Coinheritance of BRCA2 and CYLD genes may lead to new treatment options for certain cancers.

Seven new genetic risk areas for prostate cancer were found.

Frontal fibrosing alopecia may run in families.

Androgenetic alopecia is more common in males, can be influenced by lifestyle, and may be linked to other skin issues.

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

Prenatal genetic diagnosis may not predict MELAS syndrome severity in offspring.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

Thorough history and examination are crucial for diagnosing genetic disorders like juvenile polyposis and hypomelanosis of Ito.

Men who experienced baldness at age 20 may have double the risk of getting prostate cancer.

Baldness is common in Korean men (60.5%), and those with a family history are 3.1 times more likely to have hairline recession.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Certain genetic markers on the Y-chromosome may influence prostate cancer risk in Iraqi males.

New genes linked to male pattern baldness were found on chromosome 20p11.

Recognizing minor skin lesions can help identify serious cancer syndromes.

The condition is likely inherited in an autosomal-dominant pattern.

Certain mutations in the PADI3 gene may increase the risk of developing a type of scarring hair loss common in women of African descent.