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Lymphangiohemangioma, also called lymphatic-venous or venolymphatic malformation, is a rare malformation of the lymphatics, with vascular elements.
Cavernous malformation (CM) (also known as cavernous angioma, cavernous hemangioma, and cavernous vascular malformation) is a type of angiographically occult vascular malformation.
The Chiari malformation is a structural defect in the cerebellum, which is described comprehensively at a clinical level, but its repercussions are not fully understood in the development and learning processes.
Congenital cystic adenomatoid malformation is a rare bronchopulmonary malformation located in the lung.
Introduction The Chiari I malformation is a rare pathological condition that is characterized by a downward herniation of the cerebellar tonsils and brainstem through the foramen magnum.
That malformation is a form of porencephaly.
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In the case of BRAHD, the primary malformation is an intrinsic error of renal development with the other features of Potter syndrome resulting from intrauterine deformation due to oligohydramnios.
A less common malformation is an aberrant left subclavian artery, which may occur in conjunction with a persistent right aortic arch or alone.
Congenital inner ear malformation is an uncommon fistula route, which can be misdiagnosed even regular CT (usually cut every 5 mm) is performed without performed high resolution CT (usually cut every 1 mm).
Ethnicity per se was no longer a predictor of mortality once congenital malformations were included in a logistic regression model, but the interaction of Bedouin ethnicity and congenital malformation was a significant predictor of mortality.
The most common cardiac malformation was a VSD, which was present in all embryos, and was associated with DORV in some embryos.
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