What is Sakati Syndrome?
Sakati Syndrome is a very rare congenital consideration which is characterized by the child having an abnormally pointed head as a result of premature closing of the cranial sutures , which is a aesculapian consideration known by the name of craniosynostosis .
to boot , there is webbing of certain fingers or toes and front of more than normal fingers . There may also be musculoskeletal deformities of the humble extremities with malformed calf . An babe with Sakati Syndrome tend to also have certain inborn cardiovascular defects as well .
There is no root cause for Sakati Syndrome found as of yet but it is believed to be caused due to random sport of genes which occurs for some unknown cause . It is an autosomal rife trait meaning that one written matter of the bad gene from either parent is enough for a child to produce Sakati Syndrome .
What are the Causes of Sakati Syndrome?
As stated , there is no known reason as to why there is development of Sakati Syndrome but researchers are of the opinion that female getting fraught at an advanced age may pass to the nestling having Sakati Syndrome but this theory has not been prove as of yet .
The best possible cause for Sakati Syndrome is believed to be sporadic variation of genes but why these mutations occur is still a matter of on-going research . This circumstance is an autosomal dominant trait meaning that one transcript of the gene from any parent is enough to induce a nipper to acquire Sakati Syndrome .
What are the Symptoms of Sakati Syndrome?
Craniosynostosis is the most prominent symptom of Sakati Syndrome with the head point upward sharply which results due to untimely closure of the cranial surgical seam . As a effect of the Sakati Syndrome , the unnatural person incline to also have sure facial characteristics include an abnormally small face , protruding eyes , elongate nose , and low set spike .
Additionally , the affected individual will also have certain musculoskeletal deformities to include abnormally short finger , webbed toe , and more than the normal number of finger , and malformed calfskin bones . The upper and lower extremity may also be shorter than normal for age in children with Sakati Syndrome .
In some example , touch individuals with Sakati Syndrome may also have developing jaw castanets , short neck andalopecia . Congenital heart shortcoming are also one of the characteristic of Sakati Syndrome .
How is Sakati Syndrome Diagnosed?
Sakati Syndrome is a medical condition that can be easily discover at the fourth dimension of nascence and upon elaborated physical examination which will clearly show the characteristics which mark the presence of Sakati Syndrome .
How is Sakati Syndrome Treated?
surgical process is the mainstay of discussion for Sakati Syndrome as most of the anomaly like craniosynostosis and centre defects can only be treated surgically . to boot surgery may be call for for chasten other musculoskeletal deformities like webbed toe and other bone abnormalities that can be seen in patients with Sakati Syndrome .
This will be to make them as self-governing as possible with deference to ambulation and their ability to carry out their activities with minimal dependency which gets severely bear on as a result of Sakati Syndrome . Additionally genetic counseling is also of much benefit for the mob who have a member with Sakati Syndrome .
