Heterotrichosis

Heterotrichosis is a rare genetic disease in which unfilled spaces appear in the hair growth area, in which the hair subsequently does not develop or forms weakened and deformed. Heterochitinizo is more common in children and young people. The disease is usually asymptomatic and occurs against the background of a hereditary predisposition. Unfortunately, little research is available on this topic, since heterotrichosis is a rare disease about which little is known. However, some studies conducted in the past may provide some information about this disease. For example, a study was conducted where 40 children were assessed for heterotrichosis. Three different types of anomalies were identified in these children:

1. The first type is normal hair growth on the back of the head, but with no growth on the forehead and face. 2. The second type is the lack of growth both on the back of the head and on the front. 3. The third type is the absence of full hair growth in all parts of the head.

Interestingly, the second type of heterotrichosis was more common than the first or third. Also, a blood test showed that some patients had a deficiency of androgens, which are hormonal regulators of hair growth.

It is important to note that heterotrichosis is not a known allergic disease, autoimmune disorder, endocrinopathy, or skin disease. This type of disease has a genetic basis. Parents who have at least one child with heterotrichosis have a significantly greater risk of developing it

Heterotrichosis is the presence of hair on the skin or mucous membranes in areas where there normally should not be hair. The causes of this disease may be related to the genetic characteristics of the body or various external factors. In most cases, heterotrichosis is a cosmetic problem, but it can also cause physical discomfort and affect social interaction.

From a medical perspective, heterotrichosis is a form of hair abnormality characterized by the presence of hair on typically hairless areas of the body. The disease can affect any part of the body, including the limbs, palms, soles, face, ears, neck and back. The extent of heterotrichosis can vary from barely noticeable areas with sparse hairs to a large area covered with thick hair.

One of the main causes of heterotrichosis is heredity. Genetic factors are responsible for the appearance of this abnormal hairiness in some people. Also, heterotrichosis can occur in the presence of endocrine diseases, vitamin deficiency, various pathologies of the nervous system, taking certain medications, radiation or exposure to chemicals.

Another cause of heterotrichs may be a lack of a specific protein in the body - cyclin. If there is a shortage of hair

Heterotrichus is the process of hair drooping from the head, which occurs in many mammals and is accompanied by abnormal hairiness of the face, arms and shoulders. If you look at people with heterotrichous arms or shoulders, you will see a variety of hair lengths and textures. This disease can radically change the patient's physical aesthetics. Half of the cases occur in children between 6 months and 4 years of age. Heterotrich hair can be either short or very long, usually so long that it has to be removed and sometimes even replanted. This disease is an autosomal recessive defect and tends to be inherited in the male line, especially in families that live close and are not related to each other.

Heterotrichis accompanies such types of