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This malformation is typically associated with hydrosyringomyelia.
This malformation (postaxial, right-dominant forelimb ectrodactyly) is almost a perfect phenocopy of R Low/- mice.
This malformation was overcome by co-treatment of miR-9 inhibitor.
This malformation gives problems of fitness for presentation and it increases the possibility of breaks and fissures, with consequent exposition of the mesocarp to fungal and bacterial infections.
This malformation was singled out as a possible cause of the MSAFP elevations as we had previously documented an association between esophageal atresia and elevated MSAFP and hypothesized that impaired swallowing might prevent reabsorption of AFAFP[ 15].
Children with this malformation are retarded and have seizures.
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This may be due to the very small number of cases involving this rare malformation.
Achieving solid arthrodesis across this congenital malformation is challenging and prone to non-union.
We read that the average life expectancy for a child with this brain malformation was two years.
- This cardiac malformation is presumably caused by 2 mechanisms.
This unusual malformation was one-off occurrence, and there were no other indications of BVD virus – associated in this herd.
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