Abstract
Introduction
Robert’s syndrome is a rare genetic disorder characterized by prenatal and postnatal growth retardation, limbs, and craniofacial defects. The limb defects are similar to those seen in Thalidomide embryopathy, hence, the disorder is also known as pseudothalidomide syndrome.
Robert’s syndrome occurs equally in both male and female baby and is common among closely related parents (parental consanguinity). Only about 150 cases have been described in the literature in the world over.
References
- National Organization for rare disorders, NORD Report. 2012
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- Socolov RV, Andreescu NI, Haliciu AM, et al. Intrapartum diagnostic of Roberts syndrome- case presentation. Rom J Morphol Embryol 2015; 56(2): 585-588.
- American Academy of Pediatrics; Committee on Fetus Newborn: Americal College of Obstetricians Gynecologists; Committee on Obstetric Practice. The Apgar score. Adv Neonatal Care 2006; 6(4): 220-223.
Corresponding Author
Dr Nidhi Kumari
PGT 3rd year, Dept of Obstetrics and Gynaecology, KMCH
DOI: https://dx.doi.org/10.18535/jmscr/v10i10.08
