Morphogenetic variability and genetic loads among patients with different expression of developmental hip dysplasia
Assuming that developmental hip dysplasia (DDH) is a genetically controlled disease, we made a hypothesis that an increased homozygosity level and genetic loads, among the patients with DDH, could be some kind of predisposition for the degree of illness expression. Using HRC-test (test for...
Main Authors: | , , , |
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Format: | Article |
Language: | English |
Published: |
Serbian Genetics Society
2017-01-01
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Series: | Genetika |
Subjects: | |
Online Access: | http://www.doiserbia.nb.rs/img/doi/0534-0012/2017/0534-00121703035M.pdf |
Summary: | Assuming that developmental hip dysplasia (DDH) is a genetically controlled
disease, we made a hypothesis that an increased homozygosity level and
genetic loads, among the patients with DDH, could be some kind of
predisposition for the degree of illness expression. Using HRC-test (test for
determination of homozygously recessive characteristics in humans) we
analyzed presence, distribution, and individual combination of 20 selected
genetically controlled morphophysiological traits among DDH patients (N=200)
and controls (N=200). Among groups of DDH patients the increase in the degree
of genetic homozygosity correlates with the degree of illness expression
(dysplasia/subluxations-39%; luxations-45%). There is significant difference
in mean HRC value between tested groups of patients with dysplasia/luxations
(p<0.05) and subluxations/luxations (p<0.05). Our results showed increase of
morphogenetic homozygosity in the group of patients with bilateral hip
dislocation (BL) (45%), compared to group with unilateral expression (UL)
(41%) and control (23.5%). There is significant difference in mean HRC value
between tested groups of patients with UL and BL (p<0.05). Also, surgically
treated patients showed significant increase of genetic homozygosity (43%)
compared to those conservatively treated (37%) and controls. We found
significant difference in mean HRC value between tested groups of patients
that were treated conservatively and surgically (p<0.05). Our results showed
increase of genetic homozygosity in the groups of DDH female patients (44%),
compared to male patients (39%), while in controls there was no difference
between gender. Female DDH patients show a significant increase in average
homozygosity of tested genetic markers (p<0.05) than male DDH patients. The
enlargement of genetic loads correlates with severity of the disease (in
studied groups of DDH patients) which may indicate some kind of
predisposition for the degree of illness expression. |
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ISSN: | 0534-0012 1820-6069 |