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Heat treatment increases hair loss in certain mice.

Our microbiome may affect the development of the hair loss condition Alopecia Areata, but more research is needed to understand this relationship.

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

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

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

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

The review says skin conditions with sterile pustules need more research for better treatments.

The document concludes that proper diagnosis and a multidisciplinary approach are crucial for managing Congenital Adrenal Hyperplasia effectively.

Some patients developed skin inflammation after obesity surgery, and a medication called dapsone helped treat it.

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.

Further research is needed to improve hair regeneration using stem cells and nanomaterials.

The document concludes that diagnosing and treating Congenital Adrenal Hyperplasia is complex and requires a team approach due to its effects on the skin and other symptoms.

A 3-year-old boy lost all his hair due to a rare reaction to phenobarbital, but it grew back after steroid treatment.

The 60-second timed hair count is a reliable and simple way to measure hair shedding at home, showing older women tend to shed more hair than younger women.

Type 1 diabetes often occurs with other autoimmune diseases, and personalized treatment based on genetics can improve outcomes.

Genetic discoveries are leading to new treatments for alopecia areata.

A woman with lupus also developed a severe skin condition linked to a genetic factor.

Certain immune system genes are linked to a higher risk of psoriasis and psoriatic arthritis, while others may offer protection.

Children's Serum Sickness-Like Reaction is often linked to antibiotics, especially amoxicillin, and involves symptoms like rash, fever, and joint issues.

Atopic dermatitis significantly lowers the quality of life for infants and their families.

Female hair loss can be diagnosed using specific trichoscopy criteria.

ALA-PDT is effective and safe for chronic X-ray dermatitis, providing complete or partial remission.

Most people with systemic lupus erythematosus have skin problems, and skin symptoms are often the first sign of the disease.

Vitiligo is not linked to coeliac disease, but a small number of alopecia areata patients may have it, suggesting they should be tested for coeliac disease.

Thyroid diseases may contribute to autoimmune skin diseases, and more research is needed on their relationship.

A gluten-free diet stopped a child's hair-eating behavior and suggested she had celiac disease.

The document concludes that parathyroid diseases have a range of clinical features and outcomes, with some conditions being treatable and others having a high risk of mortality.

The skin condition PUPP usually gets better on its own after giving birth and is unlikely to happen again in future pregnancies.