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The update highlights that non-classic congenital adrenal hyperplasia is common in women with excess male hormones, requires specific hormone tests for diagnosis, and has various treatment options depending on age and symptoms.

The document concludes that clinicians should be aware of common hair and scalp disorders in women of African descent and that more research is needed to develop effective treatments.

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.

Increased PPARGC1α relates to hair thinning in common baldness.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

Dynamic, light touch is sensed through a common mechanism involving Piezo2 channels in sensory axons.

The chapter explains that there are many genetic skin disorders affecting skin cell formation, including both common and rare types.

The study found that two enzymes linked to hair loss are located in different parts of the scalp, supporting a common treatment's effectiveness.

The document concludes that Nonclassic Congenital Adrenal Hyperplasia requires personalized treatment plans to manage symptoms and fertility, with glucocorticoids being a common therapy.

People with Lichen Planopilaris are more likely to have autoimmune diseases, especially Systemic Lupus Erythematosus, and less likely to have diabetes and some other common conditions.

About 15% of adolescent girls in a region of India have Polycystic Ovarian Syndrome, which is more common in those born by cesarean, with wisdom teeth, or with central obesity.

Cancer rates are increasing in developed countries, with estrogen, aging, low vitamin D3, and HPV infection as common causes.

Hair loss severity relates to increased miniaturization in female pattern hair loss.

YAP and TAZ proteins are necessary for the development of two types of skin cancer.

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.

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.

Manipulating the catagen and telogen phases of hair growth could lead to treatments for hair disorders.

Smad4 is important for healthy hair follicles because it helps produce a protein needed for hair to stick together and grow.

Blocking TSLP reduces skin inflammation and cell overgrowth in psoriasis.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

Female pattern hair loss has unclear causes, possibly involving genetics, hormones, and environment, and needs better treatments.

Retinoic acid helps activate hair growth in people with common hair loss by working on a specific cell growth pathway.

A gene mutation in Lama3 is linked to a common type of hair loss.

Fungal infections were the most common skin problem in North & Middle Andaman.

Deleting the Far2 gene in mice causes sebaceous gland issues and patchy hair loss.

A substance called Cell-free fat extract can effectively treat common hair loss by increasing hair growth and density.

The document concludes that hair loss is complex, affects many people, has limited treatments, and requires more research on its causes and psychological impact.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

Examining scalp tissue under a microscope helps diagnose and understand hair loss diseases.