• Shankar Dey
• Prasanna Roy

Osteogenesis Imperfecta (OI) is a rare genetic disorder characterized by brittle bones and skeletal deformities. Prenatal diagnosis of OI can be challenging, and early detection is crucial for appropriate counseling and management.High index of suspicion is necessary for the early detection of this rare skeletal deformity. Ultrasound scan of the fetus during the first trimester can detect the abnormality when done in a appropriate setting and recommended protocol.This case report presents the first trimester ultrasound detection of OI, describing the prenatal ultrasound features, subsequent post-abortal findings matched with the ultrasound imaging and confirmatory genetic testing results.

Osteogenesis imperfecta, first trimester ultrasound, prenatal diagnosis, genetic disorder, skeletal deformities

"First Trimester Ultrasound Detection of Osteogenesis Imperfecta: Prenatal ultrasound clues discussed with a case report ", International Journal of Emerging Technologies and Innovative Research (www.jetir.org), ISSN:2349-5162, Vol.10, Issue 6, page no.j527-j532, June-2023, Available :http://www.jetir.org/papers/JETIR2306961.pdf

"First Trimester Ultrasound Detection of Osteogenesis Imperfecta: Prenatal ultrasound clues discussed with a case report ", International Journal of Emerging Technologies and Innovative Research (www.jetir.org | UGC and issn Approved), ISSN:2349-5162, Vol.10, Issue 6, page no. ppj527-j532, June-2023, Available at : http://www.jetir.org/papers/JETIR2306961.pdf