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Porphyria cutanea tarda causes skin issues due to an enzyme deficiency.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

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

Patched1 helps prevent tumors by controlling cell growth.

Understanding keratinization is crucial for treating skin conditions like ichthyoses and psoriasis.

A 1-day or 3-day itraconazole treatment is effective for acute vulvovaginal candidosis, but recurrent cases may need longer treatment.

Hidradenitis Suppurativa is a chronic skin condition best treated early with surgery for better outcomes and less recurrence.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

An addax had skin cancer that spread to lymph nodes and was euthanized.

Genetic factors play a major role in acne.

Sex and sex hormones can affect brain inflammation in Parkinson's disease, with male mice being more affected and female mice showing a protective effect.

Notch signaling disruptions can cause various skin diseases.

A person was born with both a rare hairless condition and a type of birthmark, which is an uncommon combination.

Skin problems are common in Lupus patients and can indicate the disease's severity, requiring specific treatments and lifestyle changes.

New treatments and management strategies for skin conditions like melanoma and Spitz naevi were discussed at the dermatologists' meeting.

Most patients with Porphyria Cutanea Tarda had skin blisters and were often affected by hepatitis C and alcohol abuse, with differences between familial and sporadic cases.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

Basal cell carcinoma mostly starts from cells in the upper skin layers, not hair follicle stem cells.

The document concludes that the girl's hairlessness is likely inherited from her parents.

The document concludes that doctors should recognize congenital triangular alopecia to avoid unnecessary treatments, as it does not respond to steroids like alopecia areata does.

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

Aging causes sweat glands to shrink and move upward, leading to less elastic skin and more wrinkles.

The document reports the first Brazilian case of a girl with Becker nevus syndrome, characterized by skin changes, breast underdevelopment, and scoliosis.

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.

The herbal hair cream helps protect and improve hair health.

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

The topical inhibitor CUR61414 was not effective in treating basal cell carcinoma in human trials.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.