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Early diagnosis and a strict gluten-free diet are crucial for children with celiac disease to improve symptoms.

Methotrexate is not proven effective for inducing remission in ulcerative colitis.

JAK inhibitors show promise in effectively treating hair loss from alopecia areata.

Skin changes in women with PCOS are mainly due to hormonal imbalances.

UV exposure reduces Lgr6+ stem cells in mouse skin and they don't significantly contribute to skin cancer development.

The ACE1 gene variant doesn't affect long-COVID symptoms.

WWOX deficiency in mice causes skin and fat tissue problems due to disrupted cell survival signals.

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

The UK's EDS National Diagnostic Service found that early diagnosis, lifestyle advice, and regular check-ups are crucial for managing vascular Ehlers-Danlos syndrome. A combination of losartan and bisoprolol can reduce vascular events, improving survival and quality of life.

Male and female hair loss have different genetic causes.

Mitochondrial dysfunction links metabolic syndrome and inflammatory skin diseases, suggesting targeted therapies and lifestyle changes.

A new tool can analyze hair to detect changes due to hormones, genetics, and aging.

CT scans can find serious prostate cancer even when PSA levels are low.

Some lesser-known causes of PCOS include autoimmune issues, genetic mutations, and changes in the body's microbiome.

The Wnt/β-catenin pathway is important for body functions and diseases, and targeting it may treat conditions like cancer, but with safety challenges.

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

Vitamin D and its receptor may help prevent skin cancer.

Vitamin D receptor may help protect against UV-induced skin cancer.

The study concluded that immune cells attacking hair follicles cause hair loss in alopecia, with genetics and environment also playing a role, and highlighted the potential of certain treatments.

Keratin proteins are essential for keeping the cells in the human colon healthy and stable.

PTEN helps control the number and health of skin stem cells by working with the protein BMAL1.

Oxidative stress plays a significant role in alopecia areata, and new treatments may include JAK inhibitors and antioxidants.

EGCG may help treat alopecia areata by blocking certain immune responses and reducing specific harmful immune cells.

Rapamycin reduces age-related hearing cell loss in mice, but acarbose does not.

The research confirms that Hidradenitis Suppurativa is characterized by increased inflammation, disrupted skin cell organization, and abnormal metabolic processes.

Different types of cell death affect skin health and inflammation, and understanding them could improve treatments for skin diseases.