Six fetuses with normal chromosomes were found to have severe craniofacial, limb, and visceral malformations during the second trimester of pregnancy. Two of these fetuses were monozygotic twins while a third one had a healthy dizygotic twin brother. A case with familial recurrence was also observed
Fetal transverse limb defects: Case series and literature review
β Scribed by Ferha Saeed; Gowrishankar Paramasivam; Marcin Wiechec; Sailesh Kumar
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 205 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0091-2751
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β¦ Synopsis
Abstract
Purpose.
To investigate the incidence and outcome of antenatally diagnosed isolated transverse limb defects at a major tertiary center and to review the literature relevant to this rare condition.
Methods.
This was a retrospective review of all cases (2000β2009) diagnosed with an isolated transverse limb defect referred to a tertiary fetal medicine center. Isolated transverse limb defects were defined as partial or complete absence of a part of one or more limbs in the absence of other abnormalities.
Results.
Nine cases were identified. The upper limbs were affected in seven cases. The median gestational age at diagnosis was 22+5 weeks (range 21β29 weeks). The defects ranged from absence of digits to the absence of three limbs in one case. Four women opted to have termination of pregnancy. Postnatal and postmortem examination confirmed the ultrasound findings. No obvious risk factors could be identified in the majority of cases.
Conclusions.
Most cases of limb defects are believed to be secondary to a vascular insult occurring early in embryonic life. The reason for upper limb predominance remains unclear. Perinatal outcome in this series was poor with the majority of pregnancies terminated. Longβterm functional outcome depends on the severity of the limb reduction defect. Β© 2011 Wiley Periodicals, Inc. J Clin Ultrasound, 2011
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