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   Apert Syndrome: Report of a rare congenital malformation  
   
نویسنده rathore e. ,rathore a.h.
منبع pakistan journal of medical sciences - 2017 - دوره : 33 - شماره : 3 - صفحه:773 -775
چکیده    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. © 2017,professional medical publications. all rights reserved.
کلیدواژه Apert syndrome; Rare congenital anomaly
آدرس maxillo facial surgery,faryal dental college,lahore, Pakistan, foundation hospital rajana,distt: toba tek singhpunjab, Pakistan
 
     
   
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