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Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

Frontal Fibrosing Alopecia is a hair loss condition mainly affecting postmenopausal women, with unclear causes and various clinical patterns.

Oral contraceptive use may increase the risk of frontal fibrosing alopecia in women with a specific CYP1B1 gene variant.

A severe medication reaction required long treatment and led to hair loss and thyroid issues.

Portraits show women's hairlines have moved forward over time, suggesting changes in the occurrence of frontal hair loss.

Certain KIR genes in Indian SLE patients are linked to disease severity and could be biomarkers.

Different immune responses cause hair loss in scalp diseases, with unique patterns in scalp psoriasis possibly protecting against hair loss.

Non-classic congenital adrenal hyperplasia is a common disorder causing symptoms like acne and infertility, and it's managed based on symptoms, not just test results. Treatment can improve fertility and reduce miscarriage risk.

Early detection and stopping the drug are key to managing DRESS, and careful monitoring is important due to possible severe reactions.

Frontal fibrosing alopecia may be linked to genital Lichen sclerosus through an autoimmune process.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

The article suggests that patients with Frontal Fibrosing Alopecia may have more contact allergies, but it doesn't prove that allergies cause the condition.

Lupus is a complex disease that requires personalized treatment because it varies greatly between individuals.

2011 dermatology discussions highlighted stem cell hair treatments, new lichen planopilaris therapies, skin side effects from cancer drugs, emerging allergens, and the link between food allergies and skin issues.

Mice treatments didn't grow hair, a patient treatment may affect immune response, and people with hair loss often feel anxious or depressed.

Trichoscopy helps tell apart Frontal Fibrosing Alopecia and Lichen planopilaris by showing different hair and scalp features.

Topoisomerase inhibitors can cause hair loss, skin rash, hand-foot syndrome, and nail changes.

A woman with an unusual pattern of hair loss was confirmed to have Frontal Fibrosing Alopecia and treated with specific medications.

Familial frontal fibrosing alopecia is rare, mostly affects women, and often occurs between sisters or mother-daughter pairs.

Tofacitinib was more effective than apremilast in treating hair loss in a mouse model of alopecia areata.

Innate lymphoid cells type 1 may contribute to alopecia areata by damaging hair follicles.

The skin protects the body, regulates temperature, senses touch, and makes vitamin D.

An 11-year-old child with total hair loss may have a genetic autoimmune disease, and the outlook for hair regrowth is not good.

UVB radiation changes the levels of certain microRNAs in skin cells, which may affect cell survival and hair growth.

Most women with ankylosing spondylitis tested positive for HLA-B27, suggesting it's useful for diagnosis.

Certain genes are linked to the risk of developing Alopecia Areata.

Mercury allergy linked to specific genes may contribute to burning mouth syndrome, and silicon might play a role in maintaining healthy hair.

A boy with severe immune deficiency and Epstein-Barr virus died from high-grade B-cell lymphoma.

Alopecia areata can be transferred through stem cell transplants from affected siblings.

R-spondin2 may help treat hair loss, gene differences could explain baldness, a peptide's regulation is linked to psoriasis, B-defensin gene copies may affect a skin condition's risk and severity, and potential markers and targets for alopecia areata were identified.