Douira-Khomsi Wièm
Department of Paediatric radiology, Béchir Hamza Children’s Hospital, Tunis, Tunisia
* Correspondence: Khomsiwiem@yahoo.fr
A 30-year-old pregnant woman was referred to our department at 16 weeks’ gestation, a routine antenatal ultrasound identified multiple skeletal abnormalities.
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CORRECT ANSWER EXPLAINED BELOW | |
Correct Answer is: Osteogenesis imperfectaThe triad of bone shortening, decreased bone density and numerous fractures including beaded ribs is consistent with the diagnosis of osteogenesis imperfecta (OI) type II. These findings were confirmed after the medical pregnancy termination by post mortem examination including fetoplacental examination, radiographs (Image 5) and biochemical studies of cultivated fibroblasts from the fetus. DiscussionOI is a rare inherited bone disease caused by defects in type I collagen synthesis. The most widely used classification for OI distinguishes four types, based on clinical findings and disease severity, type II is the most severe form with perinatal death. It can be diagnosed by ultrasound from 14 weeks of gestation, on specific signs suchas intra-uterine growth retardation or hydramnios. Otherwise, US may show abnormalities of skull, ribs, spine or limbs: decreased echogenicity due to insufficient mineralization, deformities related to fractures, callus formation, increased bone plasticity and micromelia, especially of the femur. however, it is important to recognize that it can be difficult some times to US to distinguish between severe OI and other lethal skeletal dysplasias such as camptomelic dysplasia or thanatotropic dysplasia. ConclusionOI type II is a rare lethal pathology of the skeleton with severe abnormalities that may be identified by first trimester ultrasound. Conflicts of InterestThe author declare no potential conflict of interest. References
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CORRECT ANSWER EXPLAINED BELOW | |
Correct Answer is: Osteogenesis imperfectaThe triad of bone shortening, decreased bone density and numerous fractures including beaded ribs is consistent with the diagnosis of osteogenesis imperfecta (OI) type II. These findings were confirmed after the medical pregnancy termination by post mortem examination including fetoplacental examination, radiographs (Image 5) and biochemical studies of cultivated fibroblasts from the fetus. DiscussionOI is a rare inherited bone disease caused by defects in type I collagen synthesis. The most widely used classification for OI distinguishes four types, based on clinical findings and disease severity, type II is the most severe form with perinatal death. It can be diagnosed by ultrasound from 14 weeks of gestation, on specific signs suchas intra-uterine growth retardation or hydramnios. Otherwise, US may show abnormalities of skull, ribs, spine or limbs: decreased echogenicity due to insufficient mineralization, deformities related to fractures, callus formation, increased bone plasticity and micromelia, especially of the femur. however, it is important to recognize that it can be difficult some times to US to distinguish between severe OI and other lethal skeletal dysplasias such as camptomelic dysplasia or thanatotropic dysplasia. ConclusionOI type II is a rare lethal pathology of the skeleton with severe abnormalities that may be identified by first trimester ultrasound. Conflicts of InterestThe author declare no potential conflict of interest. References
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