Abstract:
:Febrile seizures (FS) are the most common neurological disorder in childhood and are a great stress for parents due to their dramatic clinical appearance. Using test for determination of homozygously recessive characteristics in humans (HRC test) we analyzed presence, distribution, and individual combination of 20 selected genetically controlled morphophysiological traits among FS patients (N=121) and control (N=121) to determine a possible deviation in the homozygosity level and genetic loads in the group of affected children and whether there is a predisposition to the occurrence of FS. The results of our study show a statistically significant difference in the mean values of the HRC tested ( x ¯ H R C / 20 CN = 3.2 ± 0.2; x ¯ H R C / 20 FS = 4.6 ± 0.2, t= 5.74 , p< 0.0001), as well as in the distribution and variability of two studied samples (VC=55,3%, VFS= 39,6%), which indicates a complex polygenic difference among the tested groups of subjects. The differences in the degree of genetic homozygosity and variability are also present between the genders (t Cf/FSf = 4.12; t Cm/FSm = 3.98; p <0.0001) (VCf=56.9%, VFSf= 39.3%; VCm=54.1%, VFSm=40.1%). Obtained results indicate the enlargement of recessively homozygous genetic loads in the group of children with FS which may represent some kind of predisposition for expressivity of this type of seizures.
journal_name
Biomed Res Intjournal_title
BioMed research internationalauthors
Dimitrijevic S,Cvjeticanin S,Pusica A,Jekic B,Filipovic T,Nikolic Ddoi
10.1155/2018/7845904subject
Has Abstractpub_date
2018-07-05 00:00:00pages
7845904eissn
2314-6133issn
2314-6141journal_volume
2018pub_type
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