Meier-Gorlin syndrome with ventriculomegaly and hypoplastic corpus callosum: a rarely reported congenital malformation

Meier-Gorlin syndrome (MGS) or ear-patella-short stature syndrome (MIM 224690) is a rarely reported autosomal recessive disorder having characteristic triad of microtia, short stature and aplastic or hypoplastic patella. Only 67 cases are reported. <br />We are reporting a newborn female baby...

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Bibliographic Details
Main Authors: Nabanita Kora, Kaustav Nayek, Baisakhi Soren, Rajib Das
Format: Article
Language:English
Published: Hygeia Press di Corridori Marinella 2016-02-01
Series:Journal of Pediatric and Neonatal Individualized Medicine
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Online Access:http://www.jpnim.com/index.php/jpnim/article/view/050123
Description
Summary:Meier-Gorlin syndrome (MGS) or ear-patella-short stature syndrome (MIM 224690) is a rarely reported autosomal recessive disorder having characteristic triad of microtia, short stature and aplastic or hypoplastic patella. Only 67 cases are reported. <br />We are reporting a newborn female baby with typical features of MGS along with some other features never described before, ventriculomegaly and hypoplastic corpus callosum. <br />We did x-rays of whole body (infantogram) and MRI of brain for microcephaly. <br />Ultrasonography of both knees showed absence of patellae and brain MRI showed ventriculomegaly and hypoplastic corpus callosum. <br />To our best knowledge this is the second case report of MGS in India; the first reported a MGS associated with papilledema. In previously reported cases, there was no statement regarding agenesis of corpus callosum.
ISSN:2281-0692