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Poison - Intro
01:05
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Normally the heart is located in the middle part of the thorax, in dextrocardia it is located in the right half of the thorax due to a congenital alteration and generally accompanied by situs inversus (the organs are on the opposite side of where they should be)
In transposition of the great arteries, there is an abnormal arrangement of the major blood vessels, the superior and inferior vena cava, the pulmonary artery, the pulmonary veins, and the aorta.
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Roberts syndrome is generally characterized by abnormalities of the limbs and face, including phocomelia in some severe cases, the absence of bones and muscles in the upper or lower limbs (in more extreme cases the limbs arise directly from the trunk).
Craniofacial malformations include cleft lip, cleft palate, microcephaly (head size smaller than usual), among others
The methods to be diagnosed are based on cytogenetic tests, those affected present premature separation of the centromeres and separation of the heterochromatic regions in most of the chromosomes in metaphase
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It is a congenital malformation; it presents a single facial orbit due to the failed division in the forebrain during the development of the embryo.
It is very common that there is also a dysfunctional nose, in some cases they may be underdeveloped or in other cases absent, being replaced by a proboscis, usually located in the middle of the face.
The vast majority of those born with cyclopia who manage to survive delivery have other serious defects that would make survival difficult.
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The most severe type of holoprosencephaly, the forebrain is not completely divided, characterized by the fusion of the two cerebral hemispheres and the absence of the interhemispheric fissure.
Other associated symptoms may be cyclopia, proboscis or hypotelorism
Malformations of the heart, intestines, or brachial plexus injury (myelomeningocele) may occur in other organs of the body.
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It is the lack of formation of the brain region (corpus callosum) produced by an alteration in embryonic development, it is a rare case of congenital disorder
The incidence is higher in genetic conditions such as trisomy 8 and trisomy 18
It may be accompanied by other malformations such as very small cerebral convolutions (microgyria), neuronal migration disorders or periventricular alterations.
It is not possible for the corpus callosum to be regenerated
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Cerebral Suppuration Paraguay
Pathological Goregrind from Paraguay formed in 2022,worshiping goregrind masters Lymphatic Phlegm
cerebralsuppuration@gmail.com
Our other project: carcinosis.bandcamp.com
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