| Literature DB >> 18537018 |
Rakesh Kumar1, Manoj Rawal, Shalini Agarwal, Geeta Gathwala.
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.Entities:
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Year: 2008 PMID: 18537018 DOI: 10.1007/s12098-008-0083-9
Source DB: PubMed Journal: Indian J Pediatr ISSN: 0019-5456 Impact factor: 1.967