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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.

The conclusion is that removing both ovaries is the best treatment for excess male hormones in postmenopausal women, with medication as another option, and managing insulin resistance is important for diagnosis and treatment.

PL-FUT is an effective hair restoration method for burn victims with minimal scarring and high patient satisfaction.

Two siblings were the first reported cases of inheriting both eye coloboma and loose anagen syndrome together.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

The article concludes that hair loss is a common side effect of drugs treating skin cancer by blocking the hedgehog pathway, but treatment should continue, and more selective drugs might prevent this side effect.

FoxN1 overexpression in young mice harms immune cell and skin development.

Children with HIV often have skin problems that can indicate the severity of their immune system damage.

Elderly abuse is often by family members, and doctors, especially dermatologists, can spot it by looking for unusual injuries and malnutrition.

The document concludes that hormonal biomarkers are key for diagnosing hyperandrogenemia in women and hypogonadism in men.

Some congenital hair disorders improve with age and can be managed with treatments like minoxidil, retinoids, supplements, and gentle hair care, but there's no cure.

Pannexin 3 helps skin and hair growth by controlling a protein called Epiprofin.

A mutation in the Adam10 gene causes freckle-like spots on Hairless mice.

The conclusion is that young women with excessive hair growth should be quickly tested for hormonal issues and treated to improve their social well-being.

The document concludes that hair loss is common and can be treated with medications like minoxidil or surgical options, and it significantly affects people's psychological well-being.

In a Tuscan pediatric clinic, 7.19% of children had hair or scalp disorders, with nonscarring alopecia being the most common.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Irregular menstrual cycles in exercising women may be linked to energy deficiency or hormonal imbalances, requiring careful diagnosis for proper treatment.

A baby had a rare condition with abnormal blood vessels in the brain and unusual skin and hair growth, possibly a new syndrome.

Understanding and manipulating epigenetic changes can potentially lead to human organ regeneration therapies, but more research is needed to improve these methods and minimize risks.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

ILK is essential for skin development, pigmentation, and healing.

The new SIS-PEG sponge is a promising material for skin regeneration and hair growth.

The 3D skin model is better for hair growth research and testing treatments.

People with Mucopolysaccharidoses often have skin problems like thick skin and extra hair, and recognizing these can help diagnose and treat the condition early.

Deleting Snai2 and Snai3 causes fatal autoimmunity.

Melanocytes are diverse cells important for pigmentation and skin health, influenced by genetics and environment.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

The "flying-wings" scalp flap technique is a simple, safe, and effective way to reconstruct large areas of scalp loss in children.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.