Diabetic embryopathy (Q83270): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Knowledge Architect | |||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||
Normal rank | |||
Revision as of 08:38, 15 August 2026
Diabetic embryopathy is characterised by congenital anomalies or fetal/neonatal complications in an infant that are linked to diabetes in the mother: macrosomia, cardiovascular malformations such as laterality defects (cardiovisceral and atrioventricular discordance), outflow tract anomalies, and anomalies of the endocardial cushion (complete forms of atrioventricular septal defects) and hypertrophic cardiomyopathy, which is generally benign and transient, being the more common.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_778367655 |
||
| English | Diabetic embryopathy |
Diabetic embryopathy is characterised by congenital anomalies or fetal/neonatal complications in an infant that are linked to diabetes in the mother: macrosomia, cardiovascular malformations such as laterality defects (cardiovisceral and atrioventricular discordance), outflow tract anomalies, and anomalies of the endocardial cushion (complete forms of atrioventricular septal defects) and hypertrophic cardiomyopathy, which is generally benign and transient, being the more common. |
Statements
CID11:ID_778367655
0 references
dki-india-ID_778367655
0 references
Concluído
0 references
