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Updated: Aug 15, 2026

A High-Throughput Multiplexed Screening for Type 1 Diabetes, Celiac Diseases, and COVID-19
Published on: July 5, 2022
[The child from families with type 1 diabetes]
Renata Wasikowa1, Dorota Suchańska, Danuta Suchańska
1Katedra i Klinika Endokrynologii i Diabetologii Wieku Rozwojowego AM we Wrocłlawiu.
Insights
Type 1 diabetes poses a significant teratogenic risk, increasing congenital defect likelihood by 3-5 fold. Hyperglycemia is the primary cause, leading to various birth defects and neonatal complications.
Area of Science:
- Endocrinology
- Teratology
- Neonatology
Context:
- Type 1 diabetes is a significant risk factor for congenital anomalies.
- Genetic predisposition plays a role in Type 1 diabetes development.
- Maternal hyperglycemia during pregnancy is a key teratogenic factor.
Purpose:
- To highlight the teratogenic risks associated with Type 1 diabetes.
- To outline the spectrum of congenital defects and neonatal complications.
- To emphasize the need for continuous medical surveillance for high-risk infants.
Summary:
- Type 1 diabetes is linked to a 3-5 fold increased risk of congenital defects.
- Central nervous system, skeletal, urinary, and digestive systems are commonly affected.
- Neonatal complications include macrosomia, hypocalcemia, hypertrophic cardiomyopathy, and respiratory distress.
Impact:
- Informs healthcare providers about the critical need for glycemic control in diabetic pregnancies.
- Underscores the importance of prenatal screening and monitoring for congenital anomalies.
- Guides management strategies for infants born to mothers with Type 1 diabetes.
Abstract:
Diabetes type 1 is observed in individuals with a genetic predisposition to the disease. Observed is a 3-5 fold risk for congenital defects, therefore diabetes type 1 is one of the highest known teratogenic risk factor. The main factor responsible for the development of congenital defects is hyperglycemia. Observed are congenital defects of the central nervous system, the bones, urinary and digestive tract. Characteristic is macrosomia. Observed are hypocalcemia, hypomagnesemia, polycythemia, hyperbilirubinemia, hypertrophic cardiomyopathy, respiratory disturbances. Children from families with diabetes type 1 are at high risk for the development of the disease in the newborn period, additional diseases. They must be in permanent medical control.
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