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A specific gene variant (rs4833095) is linked to a higher risk of alopecia areata in Koreans.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

The cause of alopecia areata is likely a mix of genetics, immune system issues, and environmental factors, with more research needed to understand it fully.

Alopecia areata involves persistent gene abnormalities and immune activity, even in regrown hair, suggesting a risk of relapse.

Hair loss in certain young mice is linked to a specific gene and can be caused by lack of iron.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

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.

The document concludes that androgenetic alopecia is common, has a genetic link, and can be diagnosed and treated with medications like finasteride and minoxidil.

The guidelines suggest using various treatments, including antidepressants and steroids, for alopecia areata and discuss the condition's genetic and immune aspects.

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

A rare genetic disease causes rickets and often hair loss in young children, which can improve with specific treatments.

A mutation in the KRT82 gene is significantly associated with Alopecia Areata.

New factors in female hair loss include genetics, hormones, stress, and inflammation; future treatments should also focus on these areas and consider the patient's emotional well-being.

Children's hair loss can have various causes, including infections, autoimmune issues, physical stress, nutritional problems, and genetic factors.

Alopecia Areata affects people of all ages worldwide, is likely caused by genetic and environmental factors, and can lead to stress and depression, highlighting the need for treatments that address both physical and mental health.

A 12-year-old girl's hair loss was linked to a rare genetic condition called ALX4-related frontonasal dysplasia.

Alopecia areata causes sudden hair loss, has genetic links, and can be managed but not cured.

Congenital alopecia areata may have genetic links and topical corticosteroids are an effective treatment.

A girl with a rare genetic condition affecting hair and nails also developed a common type of hair loss, suggesting a possible genetic link.

Alopecia areata is now understood to be driven by genetic and immune factors.

Hair pattern in androgenetic alopecia overlaps with scalp and bone demarcations, with distinct gene profiles affecting susceptibility.

Society's pressure to have children later in life favors genes that increase the risk of early baldness in male offspring.

AGA is caused by genetics and androgens, treatable with finasteride and minoxidil.

Certain genetic markers on chromosome 20 are linked to hair loss in the Han Chinese from Yunnan.

Baldness is more common in Chinese men than women, increasing with age, and is influenced by genetics.

PUVA treatment is generally ineffective for alopecia areata.

Male pattern hair loss is genetic and influenced by hormones, with treatments like minoxidil and surgery available.

E211 G>A gene linked to lower risk of severe prostate cancer and hair loss.

Hair loss gene found on chromosome 3q26.