What is a child syndrome?
Congenital hemidysplasia with erythoderma ichthyosiform or child syndrome is an unusual genetic disorder. Patients with this condition experience a lack of development on the one hand, usually on the right side, and may have medical complications in the case of internal organs. Girls are most likely to develop child syndrome due to the pattern of genetic inheritance. The rarity of the condition is considered minimal during pregnancy unless there is a family history to consider. They have unusually low cholesterol and also experience the accumulation of products that the body should normally rinse, which seem to grow in fetal development and after birth. Usually, signs of a child syndrome in a very small age are easy to detect. Especially along the folds as on the elbows. One or more limbs may also be unusual; For example, the patient may miss fingers and fingers or whole limbs. Sometimes the lack of development includes internal organs on this side, which may lead to heart, lung and kidney problemsInami. Some tests can confirm the diagnosis of the child's syndrome if the doctor wants to be absolutely certain of the patient's condition.
The exact mechanism involved in the development of the child's syndrome is not fully understood. It is a feature bound to X, associated with chromosomes x carried by women, and therefore girls appear more often in girls. Patients with this condition have a demonstrable problem with the genes involved in cholesterol production, but the exact reason why low cholesterol and the accumulation of by -products causes insufficient development to be unknown. Research includes attempts to accurately understand how this is a storyline and develop better treatment options for patients.
Since 2011, there has been no medicine for this condition. Treatment of a child syndrome focuses on mastering symptoms and maintaining the patient's comfort. This may include surgery, prosthetics for comfort and physical therapy. Some patients require mobility aids and help with themby which tasks of everyday life. The skin may also require treatment to solve irritated patches and reduce pain and tenderness.
Some patients consider it useful to join supporting groups and connect with other people who have similar conditions. The rarity of the child syndrome can make it difficult to meet other patients, but other genetic conditions can cause similar skin and skeleton problems. People living with these conditions can have tips and advice for patients and parents with concern.