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Foxi3 expression in developing teeth and hair is controlled by the ectodysplasin pathway.

Recent progress has been made in understanding inherited hair and nail disorders.

Propranolol can cause reversible hair loss.

High androgen levels and genetic factors likely cause Becker's nevus and related symptoms.

XEDAR triggers a specific signaling pathway in cells.

Oncogenic K-ras causes rapid cancerous changes in the mouth's lining.

EDA signaling is linked to skin disorders, various cancers, and liver disease.

Patients with both connective tissue disease and acid reflux are more likely to have certain symptoms and physical signs.

Three dogs with a rare skin condition improved with treatment.

The document explains the genetic causes and characteristics of inherited hair disorders.

The conclusion is that different types of hair loss in dogs and cats can be cosmetic or serious, and affected animals should not be bred.

Three related Persian cats have a rare, likely hereditary skin condition causing hair loss and poor coat quality, with limited treatment options.

New gene mutations linked to skin conditions were found, bacteria and chemicals may worsen acne, a dog mutation could exist in humans, virus-like elements might be involved in psoriasis, and a vitamin D3 treatment doesn't prevent chemotherapy-related hair loss.

Topical Imiquimod may fight vascular tumors by affecting blood vessels or the immune system, low iron might be linked to some hair loss, removing the top skin layer helps vitamin C get in, genetic testing helps diagnose skin conditions, and too much iron could worsen skin inflammation.

Six genetic conditions are often linked to complete scalp hair loss in children.

The document adds two cases of Gomez-Lopez-Hernandez syndrome and suggests including trigeminal anesthesia and scalp alopecia as key diagnostic criteria.

Minoxidil does not work to inhibit lysyl hydroxylases in newborn mouse lungs.

Understanding and managing side effects of hedgehog pathway inhibitors can improve treatment for advanced basal cell carcinoma.

Kampo medicine can help treat general fatigue from long COVID.

Hair loss in Cronkhite-Canada syndrome may be caused by autoimmune factors, not just stress or malabsorption.

Frizzled receptors are essential for various body development processes and maintaining certain body functions.

Genetic screening is crucial for accurately diagnosing APS-1 due to its varied symptoms.

Adverse events from vismodegib can be managed effectively to ensure optimal treatment.

Sonidegib and vismodegib are similarly effective for advanced basal cell carcinoma, but sonidegib might have a slightly better safety profile.

The document concludes that side effects from Smoothened inhibitor drugs for skin cancer are reversible and can be managed with a team approach to maintain quality of life.

Permanent hair removal with lasers may cure itchy black hair bristles on the back.

Cronkhite-Canada syndrome can be diagnosed without gastrointestinal polyps if there is severe mucosal atrophy and edema.

Conditioned media from mesenchymal stem cells show promise for tissue repair and disease treatment, but more research is needed on their safety and effectiveness.

Long COVID in Japan involves persistent symptoms like fatigue and may be caused by lasting organ damage and prolonged inflammation, with vaccination as a potential treatment.

Recombinant thrombomodulin can effectively treat severe complications in Cronkhite-Canada syndrome.