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The document concludes that ongoing research using animal models is crucial for better understanding and treating Alopecia Areata.

Certain genetic variations in IL18 may increase the risk of alopecia areata in Koreans.

Certain gene variations in the Vitamin D Receptor are linked to higher risk of female hair loss.

Most patients with Porphyria Cutanea Tarda had skin blisters and were often affected by hepatitis C and alcohol abuse, with differences between familial and sporadic cases.

Certain ESR1 gene variations may affect hormone levels and fat distribution in women with high male hormone levels.

Certain surgical methods are better than routine incision for hidradenitis suppurativa, topical clindamycin and acitretin are effective treatments, men with HS have a risk of skin cancer, HS patients are more likely to die from heart problems, and specific genetic markers are linked to treatment response.

Alopecia areata is an autoimmune condition causing hair loss due to the immune system attacking hair follicles, often influenced by genetics and stress.

Polycystic Ovary Syndrome likely starts in childhood and may be genetic and influenced by early hormone exposure.

Some women with PCOS have CYP21 mutations and IRS1 variants, but these genetic factors are not major contributors to PCOS.

WNT10B is linked to cancer development and affects survival and disease progression in various cancers.

Anorexia Nervosa and Bulimia Nervosa are complex eating disorders with increasing incidence among young females, significant morbidity, and varying mortality rates, requiring more research for better treatment.

Higher testosterone levels can increase the risk of certain diseases like type 2 diabetes in women and prostate cancer in men, but can also protect against autoimmune diseases and hair loss. It also affects body fat and bone density.

Hypothyroidism may cause certain types of hair loss.

People with polycystic ovary syndrome have a higher chance of having chronic thyroiditis.

Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

Mexican patients had a lower incidence of skin reactions to drugs and no significant link between these reactions and the TNF2 gene variant.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

Using special RNA to target a mutant gene fixed hair problems in mice.

Neuroactive steroids may affect the risk and treatment of alcohol use disorders.

Men with Kennedy disease have less chance of hair loss.

People who carry the 21-Hydroxylase Deficiency gene are not more likely to have excessive male hormone levels.

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

Lichen Planus is a less common condition affecting skin and mucous membranes, with various types and associated risk factors, challenging to diagnose, significantly impacts life quality, and may have a risk of cancerous changes in oral lesions.

High levels of the protein Flightless I worsen ulcerative colitis symptoms in mice.

Vav2 changes how hair follicle stem cells' genes work as they age, which might improve regeneration but also raise cancer risk.

High blood pressure drugs often cause skin lupus, stopping the drug usually helps. A vaccine helps prevent genital herpes and HPV-16. More frequent light therapy clears psoriasis faster. No link was found between low iron and chronic hair loss.

Longer CAG and GGN repeats increase alopecia risk, but no significant link to post-finasteride syndrome found.

The mtDNA N haplogroup is linked to a higher risk of late-onset lupus and specific symptoms in Han Chinese women.

People with alopecia have a higher risk of thyroid cancer.

Lower testosterone levels in men may be linked to a higher risk of severe coronary artery disease.