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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.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

Different genes are active in dogs' hair growth and skin, similar to humans, which helps understand dog skin and hair diseases and can relate to human conditions.

Nagashima-type palmoplantar keratosis in Asians is caused by a SERPINB7 gene mutation.

Natural gene therapy shows promise for treating skin disorders like epidermolysis bullosa.

A cross-bred lamb with severe skin and movement issues had ichthyosis fetalis but normal vitamin A levels.

The meeting highlighted the importance of genetic testing and multidisciplinary approaches in pediatric dermatology.

Mutations in NIPAL4 cause skin issues by disrupting lipid layers, but some improvement is seen with topical treatment.

Keratosis pilaris is often linked to genetic mutations and causes skin and hair abnormalities, regardless of those mutations.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

Experts discussed treatments for skin conditions in children, emphasizing hydration, cautious medication use, and early intervention for infections.

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

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

New treatments targeting specific genes show promise for treating keratin disorders.

The nude gene causes skin cell overgrowth and improper development, leading to hair and urinary issues.

European guidelines recommend regular eye and ear exams, skin care, vitamin D supplements, and cautious use of medications for managing congenital ichthyoses.

Changes in keratin affect skin health and can lead to skin disorders like blistering diseases and psoriasis.

Topical vitamin D is useful for some skin conditions but not effective for others, and more research is needed.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

The document says that treating the root cause of hair follicle damage is crucial to prevent permanent hair loss, and treatment options vary.

Gene therapy shows promise for treating skin disorders and cancer, but faces technical challenges.

Vitamin D is crucial for skin health and managing skin diseases.

The document is a detailed medical reference on skin and genetic disorders.

The document is a detailed guide on skin conditions and treatments for dermatologists.

The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

Experts met to improve care for ichthyosis patients in Spain.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.