Sentence examples for abnormality where from inspiring English sources

Type I is an isolated abnormality where abnormal tangential and/or laminar cortical architecture is present.

However, our poll shows a clear majority in Northern Ireland in favour of access to abortion in the cases of rape (69%), incest (68%) and fatal foetal abnormality (where the foetus has no chance of surviving outside of the womb, 60%).

Polyostotic fibrous dysplasia was first described by Lichtenstein [1], as a skeletal abnormality where the medullary cavities of multiple bones were filled with 'gritty, greyish white fibrous tissue containing trabeculae of newly formed primitive bone'.

The Nazi monstrosity in Apt Pupil is structured through sexual "abnormality", where a series of binary dichotomies are introduced: "normal versus monstrous, heterosexual versus homosexual, and healthy versus sick".

The "NIPT" blood test results had come back to indicate that the fetus had tested positive for Monosomy X. Monosomy X (also known as Turner Syndrome) is a chromosomal abnormality where a female fetus has only one complete X sex chromosome.

Deontay distinctly remembered going to the doctor for a regular check up and being told that his daughter would be born with spinal bifida, a birth abnormality where there's an incomplete closing of the backbone and membranes around the spinal cord.

No abnormalities where observed when stimulating the left foot and hand.

Proportions of congenital anomalies did not vary significantly by maternal age or deprivation scores except for chromosomal abnormalities, where the proportion increased significantly with maternal age.

These cells frequently had bipolar spindles, however 60% of those spindles exhibited remarkable abnormalities where centrosomes appeared to have detached from the poles.

The controls were selected from consecutive patients undergoing MRI examinations for indications unrelated to headaches or CSF flow abnormalities where the MRI examination was seen to be without structural abnormality.

It has quickly gained attention through the rapid introduction of next-generation sequencing approaches in the domains of cancer and pediatric congenital abnormalities, where the objective is to identify one or a few rare mutations that may explain the pathology.