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Hidradenitis suppurativa is a chronic skin condition more common in women, linked to genetics and lifestyle factors, and associated with various other health issues.

Oral isotretinoin temporarily improved skin symptoms in a child with IFAP syndrome.

Treat hair loss with finasteride, minoxidil, or surgery; consider side effects and severity.

The conclusion is that better understanding and more research are needed to effectively manage follicular and scarring disorders in skin of color, with an emphasis on patient education and cultural awareness.

Oral contraceptives lower testosterone levels in women, especially those with certain genetic traits, and may be linked to increased breast cancer risk.

Some women with PCOS have rare genetic variants linked to the condition.

Childhood ptosis can vary from a minor cosmetic issue to a serious condition and may signal other health problems.

Cannabinoids like CBD and THC may help treat non-cancer skin diseases, but more research is needed.

The document suggests a new model for evaluating public research that better captures the full value of knowledge creation and use, using PCOS research as an example.

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

Keratosis pilaris is a common skin condition where hair follicles get clogged with keratin, mostly on the arms and thighs.

Pregnant women with PCOS have higher levels of Neurokinin B in the placenta, especially with female babies.

Ovulation disorders are a major cause of infertility and menstrual problems in women.

The document concludes that certain mutations may contribute to the inflammation in hidradenitis suppurativa and suggests that targeting TNFα could be a treatment strategy.

A girl with hereditary chorea, likely Huntington's disease, had her condition worsened by lupus.

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

First Korean case of Cronkhite-Canada syndrome with colon cancer and serrated adenoma.

Male pattern baldness is mostly inherited, involves many genes, and is linked to other traits like early puberty and strong bones.

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

DNA markers can predict physical traits for forensic use, but there are ethical and technical challenges.

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

A new hair transplant method suggests freezing and storing dense hairs for future use to address severe hair loss.

The document summarizes skin and immune system disease findings, especially related to AIDS, from the 1980s.

The research found that certain genes are linked to male pattern baldness, but these same genes do not affect female pattern hair loss.

Genetically repaired stem cells may treat certain genetic diseases, Th17 cells are key in fighting systemic fungal infections, hair loss in AGA is due to progenitor cell loss, and α-synuclein transfer might contribute to Parkinson's disease progression.

MC4R gene variants not linked to female hair loss.

Gene linked to common hair loss found, may lead to new treatments.

No link found between new male baldness genes and female hair loss.

A genetic test can identify people at risk of male pattern baldness early, allowing for quicker treatment.