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Male-pattern hair loss is largely influenced by genetics, with key genes identified.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

Neuregulin3 affects cell development in the skin and mammary glands.

Four new cases of Bachmann-Bupp syndrome suggest potential for targeted treatment.

Early genetic testing and JAK inhibitors can help treat systemic inflammation in SAVI patients.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Different PCOS subgroups have similar metabolic features, but those without menstrual problems have milder issues.

Biologic therapies can cause various adverse events, but allergy/immunology clinicians can manage them.

Researchers identified five new potential targets for leishmaniasis treatment, suggesting repurposing existing drugs could be effective.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

Injecting triamcinolone into the eyebrow area may help eyelash regrowth in alopecia areata patients.

Transverse sections are better for non-scarring hair loss, vertical sections are better for lichen planopilaris, and either method works for other scarring hair loss types.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

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

The research provides a gene-based framework for hair biology, highlighting the Hippo pathway's importance and suggesting links between hair disorders, cancer pathways, and the immune system.

Pangolins have lost some skin-related genes, but kept others, leading to their unique scales and skin features.

Mice without the vitamin D receptor have bone issues and other health problems, suggesting vitamin D is important for preventing various diseases in humans.

Foxp3 is crucial for regulatory T cell function, and targeting these cells may help treat immune disorders.

Eating 500 fewer calories a day and making lifestyle changes can improve PCOS symptoms and reduce diabetes risk; more research is needed on its causes and treatments.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

Finasteride reduces Tourette syndrome symptoms, but results may be limited due to potential biases.

Three new types of a skin blistering disease were found, caused by specific gene mutations.

Finasteride may help reduce symptoms in male Tourette syndrome patients.

The conclusion suggests that prostate cancer should be classified by castration status and that new therapies targeting androgen receptor signaling show promise.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

Small changes in hormones can significantly impact health, showing the importance of sensitive testing for chemicals that disrupt hormones.

Spermidine helps protect against aging by preserving telomere length.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in patients with Tourette syndrome.