IJCRRI Journ Cur Res ReInternational Journal of Current Research and ReviewI Journ Cur Res Re2231-21960975-5241Radiance Research Academy1312HealthcareMEIER-GORLIN SYNDROME- A VERY RARE CONGENITAL MALFORMATION KendreVidyadeviBhattadShital18022013101103This article is copyright of Popeye Publishing, 20092009This is an open-access article distributed under the terms of the Creative Commons Attribution (CC BY 4.0) Licence. You may share and adapt the material, but must give appropriate credit to the source, provide a link to the licence, and indicate if changes were made.

The Meier-Gorlin syndrome or ear, patella, short stature syndrome (MIM 224690) is a rare autosomal recessive disorder. It is characterized by severe intrauterine and postnatal growth retardation, microcephaly, bilateral microtia, and aplasia or hypoplasia of the patella. Despite the presence of microcephaly, intellect is usually normal (1). This case study discusses a case on Meier-Gorlin Syndrom.