HOME ABOUT US INSTRUCTIONS SUBMISSION REGISTER ADVERTISE CONTACT

PAST ISSUESCURRENT ISSUE

Volume 5, Number 4 (December 2010) , 303-306

Case Report

Sudanese infant with Fraser syndrome

Aamir Yassin1*, Somaya Al-asad2, Sausan Abdulmonim3, Amani Hashim3, Awadallah Hassan2.

 

 

Abstract:

We are reporting here a case of Fraser syndrome which is a very rare autosomal recessive disorder characterized by cryptophthalmos, cutaneous syndactyly, craniofacial dysmorphism, malformation of the upper airways and genitourinary tract. Diagnosis of Fraser syndrome is based on clinical signs.

Key wards:  Fraser symdrome (FS), cryptophthalmos (CO), syndactyly

 

1. Registrar of pediatrics, OIU, Khartoum Sudan.

2. Departm of pediatrics, Omdurman Islamic University.

3. Department of  Pediatrics, Emergency Hospital.Sudan.

    * Correspondence: amir-yasin@hotmail 


 

Copyright ęSudan JMS.
All Rights Reserved