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The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

The document concludes that systemic autoimmune diseases are complex, incurable, and require ongoing treatment and research.

NEMO syndrome and systemic lupus erythematosus are linked in a new disease association.

The document concludes that early and personalized treatment for PCOS in adolescents is crucial to manage symptoms and prevent long-term health issues.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Most adrenal cortex tumors are benign and non-secreting, but proper diagnosis and treatment are important due to the rare possibility of cancer.

Polycystic Ovary Syndrome (PCOS) is a hormonal disorder in women that can cause infertility and other health issues, and it may be improved by treatments that increase insulin sensitivity.

The document explains the causes, types, diagnosis, and treatments of hair loss, and its psychological impact, especially on women.

Multi-omics techniques help understand the molecular causes of androgenetic alopecia.

The review shows that skin symptoms like chronic fungal infections, hair loss, and skin depigmentation are key for early detection and management of APECED.

Acne is a common skin condition treated with creams, antibiotics, and emerging therapies, and it can significantly affect mental well-being.

A rare scalp condition, cutis verticis gyrata, was found in a woman with primary scarring alopecia.

Acne keloidalis nuchae is a chronic skin condition more common in African men, causing itchy or painful bumps and can lead to permanent hair loss if not treated early.

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.

Cicatricial alopecia, a permanent hair loss condition, is mainly caused by damage to specific hair follicle stem cells and abnormal immune responses, with gene regulator PPAR-y and lipid metabolism disorders playing significant roles.

Different genes are linked to various types of hair loss.

The patient with total hair loss did not regrow hair despite treatment, indicating a poor outlook for this type of hair loss.

Auto-portraits help evaluate scalp hair.

A critically ill boy experienced hair loss likely due to the stress of his medical treatments, but his hair regrew completely in 1.5 months.

Hair loss in Androgenetic Alopecia is caused by genetics, aging, and lifestyle, leading to hair follicle shrinkage and related health risks.

Better hair loss models needed for research.

Childhood hair and scalp disorders can be managed with treatments like cortisone and corticosteroids.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Four genetic risk spots found for hair loss, with WNT signaling involved and a link to curly hair.

The model suggests that scalp tension could lead to hair loss, with factors like blood vessel hardening, enlarged oil glands, and poor microcirculation also playing a role. It also hints at a possible link between skull shape and baldness pattern.

Treatment with biologic agents can significantly improve psoriasis symptoms, and blood biomarkers could potentially predict individual patient's response to treatment.

The research found that PCOS has common genetic factors regardless of how it is diagnosed and is linked to metabolic and reproductive issues.

Exposure to too much androgen before birth might cause polycystic ovary syndrome later in life.

Hidradenitis suppurativa, a chronic skin disease, can be managed with antibiotics, lifestyle changes, and in severe cases, surgery. Early diagnosis and careful planning are key, and laser treatment can be an efficient solution for mild to severe cases.

Genetic differences may affect COVID-19 deaths; anti-androgens could be potential treatment.