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

The first Japanese family with Marie Unna hereditary hypotrichosis showed hair condition improvement in a child and highlighted the risk of misdiagnosis.

DHT affects hair follicle cells by changing microRNA levels, leading to less cell growth and more cell death.

Stress may contribute to hair loss in alopecia areata by affecting immune responses and cell death in hair follicles.

Certain immune cells contribute to skin autoimmune diseases, and some treatments can reverse hair loss in these conditions.

Activating Nrf2 can help protect against hearing loss.

CRISPR/Cas9 has improved precision and control but still faces clinical challenges.

Antigen presenting cells around hair follicles are crucial in SLE-related hair loss.

5α reductase type 2 enzyme mutation and oxidative stress may increase androgenetic alopecia risk in Egyptians.

Yellow dots look different in various hair loss conditions and can help diagnose them.

The document concludes that detailed clinical descriptions of seven family cases help understand dominant dystrophic epidermolysis bullosa's symptoms and inheritance.

TGase 3 helps build hair structure by forming strong bonds between proteins.

Thyroid diseases may contribute to autoimmune skin diseases, and more research is needed on their relationship.

The document concludes that various signaling pathways and genetic factors are crucial for chicken feather development, affecting poultry quality.

A rare endocrine disorder, APS 1, was diagnosed in a 26-year-old man in Bangladesh.

Finasteride can reduce fertility in some men, but stopping it increases sperm count.

PCOS may be influenced by factors in the blood, not just the ovaries.

Androgen therapy can help with symptoms like low libido in women, but more research is needed to understand its long-term safety and effects on health.

New compounds show promise for treating hair loss, enlarged prostate, and prostate cancer, with some being more effective and having different side effects than current treatments.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

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.

Genes linked to fibrosis are more active in people with central centrifugal cicatricial alopecia.

Deleting Smad4 and PTEN genes in mice causes rapid, invasive stomach cancer.

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.

Certain Ayurvedic herbs may help manage premature greying of hair.

Trichoepitheliomas can be hard to distinguish from other skin conditions and often start in teenage years.

Certain drugs that block specific enzymes can help treat prostate diseases.

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

Animal models, especially mice, are essential for advancing hair loss research and treatment.

Fetal cells could improve skin repair with minimal scarring and are a potential ready-to-use solution for tissue engineering.