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A rare skin disease namely Ichthyosis Vulgaris

por Mattie Cullen (07/07/2021)


A rare skin disease namely Ichthyosis Vulgaris _ skin disease that is rarely affected by people is there a cure for this skin disease and what is the cause of this rare skin disease. Every human being is gifted with skin which acts as an outermost protective device. however, the skin can develop problems, conditions, or diseases, interfering with its appearance and function.

For example dermatitis, eczema, acne, and many more. but the Example mentioned that it can be cured or controlled by certain treatments. but there is also a skin disease that is classified as rare and may not have been heard of before, namely ichthyosis vulgaris.

Ichthyosis itself is a heterogeneous group of skin diseases characterized by scaling or desquamation (release of epithelial elements, especially skin, in the form of scales or fine sheets) in the skin. the purpose of the scaling indicates the differentiation of the epidermal layer Types of Skin Diseases and How to Overcome Them the skin.

The estimated prevalence of ichthyosis vulgaris in Asia is 3.0 percent and the incidence rate is 1: 100. The initial incidence of ichtyosis vulgaris disease can be experienced from 3 to 12 months of age with the same incidence between men and women caused by mutations in the profilaggrin coding gene which is the raw material for filaggrin protein, resulting in loss or reduction of filaggrin and its raw material, profilaggrin.

there is no cure for congenital ichthyosis vulgaris. but treatment for patients is symptomatic focusing on improving scale and dry skin. If anyone experiences symptoms, immediately consult a doctor so that they can get prompt treatment.

Ichthyosis itself is a heterogeneous group of skin diseases characterized by scaling or desquamation (release of epithelial elements, especially skin, in the form of scales or fine sheets) in the skin. the purpose of the scaling indicates the differentiation of the epidermal layer of the skin.

The estimated prevalence of ichthyosis vulgaris in Asia is 3.0 percent and the incidence rate is 1: 100. The initial incidence of ichtyosis vulgaris disease can be experienced from 3 to 12 months of age with the same incidence between men and women caused by mutations in the profilaggrin coding gene which is the raw material for filaggrin protein, resulting in loss or reduction of filaggrin and its raw material, profilaggrin.

there is no cure for congenital ichthyosis vulgaris. but treatment for patients is symptomatic focusing on improving scale and dry skin. If anyone experiences symptoms, immediately consult a doctor so that they can get prompt treatment.