MECKEL-GRUBER SYNDROME - A CASE REPORT
Keyword(s):
AbstractMeckel Gruber syndrome (MGS) is a rare lethal autosomal recessive disorder. It is characterized by triad of features having occipital meningoencephalocoele, polycystic kidneys and post-axial polydactyly. We report a rare case of MGS which was diagnosed by antenatal ultrasound examination and confirmed later when aborted at 21 weeks of gestation.
2017 ◽
Vol 5
(1)
◽
pp. 262
2016 ◽
Vol 4
(1)
◽
pp. 290
2020 ◽
Vol 9
(7)
◽
pp. 3063
2019 ◽
Vol 8
(7)
◽
pp. 2919
2011 ◽
Vol 30
(10)
◽
pp. 1724-1727
◽
2011 ◽
Vol 2011
◽
pp. 1-3
◽