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Semilobar holoprosencephaly in Seckel syndrome
Rakesh Kumar1, Manoj Rawal, Shalini Agarwal
1Department of Pediatrics, Pt. B.D. Sharma Postgratuate Institute of Medical Sciences, Rohtak, Haryana, India. drangural@yahoo.com
Indian Journal of Pediatrics
|June 10, 2008
Abstract:
Seckel syndrome is a rare genetic disorder with autosomal recessive inheritance. It is associated with many CNS anomalies along with involvement of other systems. We present a case of Seckel syndrome with semilobar holoprosencephaly as associated CNS anomaly, which to the best of our knowledge has not been reported earlier.
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