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Men are more likely to get infectious skin diseases, while women are more prone to autoimmune and pigment-related skin conditions, influenced by biological and environmental factors.

Gonadal dysgenesis, like Turner's and Klinefelter's syndromes, negatively affects bone health, but hormone treatments can help.

Genetics play a role in acne, but how exactly they contribute is not fully understood.

The document concludes that identifying the cause of amenorrhea is crucial for proper treatment.

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

High lactate dehydrogenase activity is not necessary for the growth of squamous cell carcinoma.

Cells from a skin condition can create new hair follicles and similar growths in mice, and a specific treatment can reduce these effects.

Mice can correct hair follicle orientation without certain genes, but proper overall alignment needs those genes.

Amenorrhea is when a woman doesn't have periods, with primary amenorrhea starting by age 15 or within five years of breast development, and secondary amenorrhea when periods stop for three months. It affects 3-4% of women not pregnant, breastfeeding, or in menopause, mainly due to polycystic ovary syndrome, hypothalamic amenorrhea, hyperprolactinemia, and ovarian failure.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Infertile men are more likely to produce sperm with abnormal chromosome numbers, which can affect pregnancy success and embryo health.

Cholesterol balance is important for hair health, and problems with it can lead to hair loss conditions.

Blocking the FGF5 gene in sheep leads to more fine wool and active hair follicles due to changes in certain cell signaling pathways.

People with myotonic dystrophy type 1 have a higher chance of getting skin tumors, including melanoma.

Bimatoprost can cause longer, thicker, darker eyelashes and eyebrows.

Amenorrhea, or the absence of periods, should be evaluated by age 15 or within five years of early breast development, and is most commonly caused by conditions like polycystic ovary syndrome and hypothalamic amenorrhea.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

The document says that treating the root cause of hair follicle damage is crucial to prevent permanent hair loss, and treatment options vary.

Lupus panniculitis of the scalp causes linear hair loss and needs ongoing treatment to prevent recurrence and lupus.

The document says menstruation is important for women's health, discusses menstrual disorders, and suggests personalized treatment options.

Hair follicle regeneration may slow tumor growth.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

In vivo lineage labelling is better than in vitro methods for identifying and understanding stem cells.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.

New markers and pathways have been found in skin tumors, helping better understand and diagnose them.

The study found that the most common repigmentation pattern in children with vitiligo is a combination of patterns, with a new medium spotted pattern identified.

Acitretin significantly reduced inflammatory attacks in a woman with Naevus Comedonicus Syndrome but caused side effects.

SV40 T antigen in hair follicles causes abnormal hair and health issues in mice.

No clear link between androgen receptor variation and hair loss, but more research needed.

Men are more likely to have severe respiratory viral infections like COVID-19 due to hormonal and genetic differences, while women generally have stronger immune responses.