Lipoidosis of the Skin and Mucous Membrane

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Lipoidosis of the skin and mucous membranes are diseases that are characterized by excessive accumulation of lipids in the skin and mucous membranes. These conditions can present with a variety of symptoms, including itching, swelling and inflammation, as well as dysfunction of the skin and mucous tissues.

There are several types of lipogylosis conditions, but one of the most common is Forge's disease. It is characterized by hypersecretion of sebum, which leads to excessive accumulation of lipids in the skin layers. This condition can lead to the formation of nodules and cysts, as well as inflammation and scarring of the skin.

Another type of lipolysis is cystic fibrosis, or cystic fibrosis. This is a hereditary disease that is characterized by damage to mucous tissues, including the gastrointestinal tract, lungs and eyes. This leads to impaired lung and skin function, which can cause complications such as respiratory failure and poor wound healing.

An identical disease affects both men and women. Its symptoms can appear at different times, from the reproductive period to old age. The development of this disease can be caused by:

- Heredity. Belongs to rare species. Frequency: 2 cases per 3800 births. The activation mechanism is autosomal recessive. In other words, the patient has at least two recessive genes. If the disease was inherited from one parent, then both genes are required. - Zygote mutation. Applies to approximately 4% of cases. It also implies the birth of a child with two recessive genes. The couple had one complete dominant gene.

If you notice symptoms of lipoidosis, you should consult a doctor for diagnosis and treatment. It is important to remember that treatment for lipoidosis can be long-term and include both drug treatment and surgical interventions. In some cases, skin grafting may be necessary to improve the appearance of the lesions.