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Male pattern hair loss is genetic and influenced by hormones, with treatments like minoxidil and surgery available.

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.

Trichoscopy is a quick and easy way to diagnose most genetic hair problems without invasive methods.

More research is needed to understand the genetic causes of Alopecia areata to develop better treatments.

Genetic data can predict male-pattern baldness with moderate accuracy, especially for early-onset cases in some European men.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Different hair growth problems are caused by genetic issues or changes in hair growth cycles, and new treatments are being developed.

The document concludes that managing non-classical congenital adrenal hyperplasia in females requires personalized treatment, genetic counseling, and a team of specialists.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

Genetic factors alone might not cause pemphigus vulgaris; other factors like birth complications and puberty may trigger it.

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

The conclusion is that hair loss from CCCA may be genetic and not solely caused by hair grooming practices.

A mother and daughter with similar hair loss conditions and identical HLA types suggest a genetic link between the conditions.

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

The review shows how to properly diagnose and treat the loss of eyebrow and eyelash hair.

Genetic defects in testosterone production can cause hormonal and developmental disorders, and more research is needed to understand androgen regulation and develop safer treatments.

Your genes, especially IL-1a, can predict how well a hair growth treatment with platelet rich plasma will work for you.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

New models predict male pattern baldness better than old ones but still need improvement.

Minoxidil, a common alopecia medication, might cause eye changes due to its properties and lack of tissue selectivity.

Certain genes may influence hair loss differently in men and women.

Genetic analysis of rabbits identified key genes for traits like coat color, body size, and fertility.

The rs6152 allele is not a good marker for baldness in the Indonesian population, but family history, age, gender, high blood pressure, and body weight are linked to the risk.

Genetic risk for PCOS can affect children's growth, metabolism, and development from early life into adulthood.

The document concludes that the development of certain tumors is influenced by genetic background and that a specific gene modification can lead to tumor regression and reduced growth.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

The document concludes that proper diagnosis and a combination of medical, hair-care, and surgical treatments are important for managing alopecia in black women.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.