Ichthyosis is a genetic disorder (it passes down from one generation to another at the time of conception of an individual). It is one of the gravest conditions caused in recent times. More than 16,000 babies around the world have been diagnosed by this condition at birth. It is a matter of serious concern and hence gene therapy (a special technique involved in changing the gene structure) is being developed to combat diseases like these.
It is caused due to the accumulation of dead and dried up skin cells in the form of thick, dry scales. This process usually appears on the surface of the skin since birth. These scales are extremely itchy in nature. The word ‘icthy’ has been borrowed from Greek literature. This word means fish. Since the scales formed during this disease look like fish scales, it is commonly known as fish skin disease. Skin, when affected with Ichthyosis, looks extremely dry and can often be confused with a case of dry skin. Make sure you look out for these scales, especially on young children, to prevent any complications.
What are the common symptoms?
Keratin is an important protein which contributes to the formation of the upper tough yet dead layer of skin. Without keratin, the skin loses its normal functions. This condition leads to the excessive accumulation of keratin in the upper layers of the skin. This is caused mainly due to the slowing down of the skin’s shedding process.
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Main symptoms include:
Scaly skin that is dry.
The appearance of small tile shaped scales.
White, gray or brown colored scales appear on dark skin.
The skin of the scalp starts flaking in the form of little white bits.
Deep crevices appear on the skin which is really painful in nature.
Elbows and lower limbs are the main locations at which these scales appear. The conditions which elevate ichthyosis include dry environments and cold climates.
Causes of Ichthyosis
The most common cause of ichthyosis is a mutation of the genes in the affected individual. This condition can be inherited from one or both parents. There are two individual genes which are present on each of the parents’ gene. One or both the genes can be inherited in the child. If one gene is present in the child then the condition is less severe while if both the genes are responsible, the condition is more severe.
Children associated with this disease are born with normal skin initially. These gradually progress into dry, flaky skin and rough characteristics. This usually develops after a period of a few years.
There are certain causes by which ichthyosis can occur without the involvement of genes. This condition is usually known as acquired ichthyosis. This is usually associated with diseases such as cancer, thyroid disease (hyperthyroidism or hypothyroidism), Hashimoto’s disease and HIV/AIDS.
Ichthyosis is certainly an annoying condition in which dry skin develops over a period of time. Look for these, especially in newborns, and report these to your pediatrician!
Tags: Ichthyosis treatment, Ichthyosis baby, Ichthyosis definition
Annie is the oldest writer at Cheap Medicine Shop and is the subject and publishing expert. She has a graduate degree in medicines along with a diploma in creative writing.