Status:
NOT_YET_RECRUITING
Result Of Karyotyping in Pediatric Patients With Congenital Anomalies and Developmental Delay
Lead Sponsor:
Assiut University
Conditions:
Congenital Anomalies
Development Delay
Eligibility:
All Genders
1-12 years
Brief Summary
The goal of this observational cross-sectional study is to study the results of karyotyping analysis for children presented with congenital anomalies and developmental delay aged 1 month to 12 years, ...
Detailed Description
Chromosomal abnormalities are the leading cause of congenital anomalies with or without neurodevelopmental delay. It is increasing in incidence worldwide and occurs in 10-15% of pregnancies and contri...
Eligibility Criteria
Inclusion
- All patients aged between 1 month to 12 years old who are presented with morphologic congenital anomalies associated with developmental delay either global DD or isolated developmental domain (cognitive, motor, speech and language or social) who are tested for chromosomal abnormalities
Exclusion
- Any patient aged between 1 month and 12 years old who is presented with Developmental Delay and congenital anomalies who didn't undergo karyotyping or other genetic testing.
Key Trial Info
Start Date :
November 1 2025
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
December 1 2026
Estimated Enrollment :
75 Patients enrolled
Trial Details
Trial ID
NCT07167017
Start Date
November 1 2025
End Date
December 1 2026
Last Update
September 11 2025
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