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Hunter syndrome is a rare genetic disorder stigmatize by a deficiency of a sure enzyme that leads to building up of complex molecules in the body . In this condition , the body is ineffectual to break down complex sugar that plays an significant role in the constitution of peel , tendon , finger cymbals and other tissues in the body . It gets deposited in various part and more and more damages them . It is overtake in families from generation to propagation . Its symptom include an magnified caput , thick nose and sassing , delayed development , husky spokesperson , joint pain , breathing problem , and many more . There is no cure known for this disease . It is mild or stern in nature and the affected child dies in 10 - 20 years in stark case . transmitted counseling is recommended in the household who have a account of this disease as prevention .
What Is The Prognosis For Hunter Syndrome?
The expectation or prognosis for Hunter syndrome depend on the severity of the disease . It can be a mild or severe type . The mild figure of this disease has a belated attack . In this form , the touched child may reach puberty and adulthood . They may have their own children . Their mental and physical ability are less deteriorated . They may still have heart disease and external respiration problems until they are active . They may survive from 20 to 60 years.(2 )
In severe variant of Hunter syndrome , children seldom reach adulthood . The disease in this form has an other onset . It may interfere with the operation of the head and the brain will lay off to work shortly . They may be hold to infirmary and cave in special care to ease their trouble . Such children do not live long . They may last up to 10 - 20 years .
Orion syndrome is a rarefied genetic disorder in which enzyme iduronate 2 - sulfatase is either absent or does not work decently . Due to lack of this enzyme , farsighted chain of refined sugar atom can not be broken down in simple molecules . These complex molecules build up in the body resulting in legal injury to various functions , thereby causing different health complaint .
hunting watch syndrome is one of the diseases belonging to mucopolysaccharides ( MPS ) . It is also eff as MPS II . It affects male child more than girl . Its symptom are not present from nativity . Its symptom start after 2 to 4 years of age as harmful complex molecules may take some time to conglomerate in the body.(2 )
What Leads To Hunter Syndrome?
Orion syndrome is an inherited disorder . The defective genes are passed on to the fry through their female parent . If bad genes are pass from the beginner to the children , the minor will rise this disease only when defective genes are drop dead from the female parent .
The defective genes can stimulate assemblage of the complex sugar molecule in the different parts of the eubstance that may result in lasting price to these component part . ( 1 )
How Do You Know If You Have Hunter Syndrome?
The symptom of Orion syndrome can be mild or severe . These symptoms do not appear presently after birthing . It starts after 2 to 4 years when enough harmful complex lucre molecules get is deposited to disturb the basic functions of the eubstance . These symptoms include-
Conclusion
Hunter syndrome is a rare genetic condition characterise by malfunction or absence of enzyme iduronate 2 - sulfatase . Its prognosis is different in different types of disease . In mild form , the small fry may exist from 20 - 60 year . In life-threatening cases , he may live 10 - 20 age only .
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