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The meeting presented findings on effective treatments for various pet skin conditions and insights into the immune responses of dogs with atopic dermatitis.

Skin symptoms are important for diagnosing infections in children.

The document concludes that understanding hair structure is key to diagnosing hair abnormalities and recommends gentle hair care for management.

The FOXN1 gene is crucial for developing immune cells and preventing immune disorders.

Oral retinoids can cause side effects ranging from mild to severe, including birth defects, and require careful monitoring and contraception.

Diabetes causes lasting cell dysfunctions, leading to serious complications even after blood sugar is controlled.

To diagnose Polycystic Ovarian Syndrome, two out of three signs—irregular periods, high male hormone levels, or cysts on the ovaries—are needed.

The document concludes that correct diagnosis and management of PCOS are important, and more research is needed on its risks and treatments.

Vitamin D3 analogs can promote hair growth in mice genetically prone to hair loss.

Dermoscopy is useful for diagnosing various skin, hair, and nail disorders and can reduce the need for biopsies.

The document explains how to identify different hair problems using a microscope.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Early adrenal gland maturation in young children can be normal, but other serious conditions should be ruled out first.

Cholesterol balance is important for hair health, and problems with it can lead to hair loss conditions.

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

Hair follicles are essential for skin health, aiding in hair growth, wound healing, and immune function.

The study concluded that androstendione and DHEA are important for diagnosing high male hormone levels in women with excessive hair growth.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

Tissue expanders effectively repair large scalp defects and restore a natural-looking scalp.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

A rare skin disorder, Ichthyosis with confetti, has no cure but treatment focuses on managing symptoms with moisturizers.

A woman got melanoma on her scalp after anti-hair loss treatment with injections.

Genetic defects in testosterone production can cause hormonal and developmental disorders, and more research is needed to understand androgen regulation and develop safer treatments.

Hypothyroidism in dogs is usually caused by immune system issues or gland atrophy, affects middle-aged purebreds most, and is treatable with medication.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

A woman with Kallman's syndrome also developed alopecia universalis, a condition not previously linked to Kallman's.

Men with a certain type of hair loss often use facial moisturizers, and a specific antibiotic treatment may help another hair condition.