Apert Syndrome: Report of a rare congenital malformation | Rathore | Pakistan Journal of Medical Sciences Old Website

Apert Syndrome: Report of a rare congenital malformation

Ehsan Rathore, Altaf Hussain Rathore


A rare case of an adult male with malformation of the skull, face, hands and feet called acrocephalosyndactly or Apert syndrome is presented. Its probable cause, features and treatment is discussed. It is a unique case who survived upto the age of 32 years without any operative intervention and adjusted in the society though he has all the stigmas of the above syndrome. We have concluded and made a point that in the adult sufferer, facial deformity is not so important and urgent for the treatment than syndactyly, which handicaps the sufferer in performing the daily routine work.

doi: https://doi.org/10.12669/pjms.333.12878

How to cite this:Rathore E, Rathore AH. Apert Syndrome: Report of a rare congenital malformation. Pak J Med Sci. 2017;33(3):773-775.   doi: https://doi.org/10.12669/pjms.333.12878

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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