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A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

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

Certain genetic variants linked to immune response increase the risk of alopecia areata in Taiwanese people.

The workshop highlighted the genetic links and psychological impacts of hair loss and skin disorders.

Atopic dermatitis may have genetic causes and can be treated with pharmacologic methods, glycerin creams, and controlling Staphylococcus aureus colonization.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

Vitamin A affects hair loss and immune response in alopecia areata.

Blood tests can help understand the genetic differences in people with alopecia areata, including how severe it is and if it's inherited.

Certain daily habits like stress, diet, and sleep can affect the severity of hair loss in alopecia areata.

Researchers found two new genetic variants linked to Alzheimer's disease.

Key genes and pathways involved in thyroid eye disease were identified, aiding potential treatment and diagnosis.

Male pattern baldness is often genetic and linked to a hormone, with treatments like finasteride and minoxidil being effective for some men.

A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.

Dandruff might be caused by changes in how hair follicles naturally release oils and an immune response to this imbalance.

The document explains the genetic causes and characteristics of inherited hair disorders.

Skin patterns form through molecular signals and genetic factors, affecting healing and dermatology.

Nonandrogenic factors like oxidative stress and microinflammation are important in hair loss progression.

Men with thinner hair from genetic hair loss may be more likely to have an enlarged prostate.

Differences in skin and gut bacteria may contribute to alopecia areata.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

The meeting highlighted the genetic basis of female pattern hair loss and various skin health insights.

Hair loss in women is genetic, diagnosed by examination and biopsy, and treated with minoxidil, finasteride, or transplantation.

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.

Hormonal interactions, especially involving DHT and estrogen, play a key role in BPH development and treatment.

PCOS management includes lifestyle changes and medications, with ongoing research into repurposed drugs for better treatment options.

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

Alopecia areata has a complex genetic basis that was not fully understood as of 2001.

Vitamin D might be involved in the development of alopecia areata and could help in its treatment.

Frontal fibrosing alopecia in families shows similar signs to individual cases and may have a genetic link.

The conclusion is that certain genetic factors and blood types may affect COVID-19 severity, but changes in ACE2 and TMPRSS2 genes are not clearly linked to it.