Paper Information

Journal:   ARCHIVES OF IRANIAN MEDICINE   october 2004 , Volume 7 , Number 4; Page(s) 307 To 309.
 
Paper: 

FRASER OR CRYPTOPHTHALMOS SYNDROME:A CASE REPORT

 
 
Author(s):  KHOURY E., GOL ALIPOUR M.J., HAIDARY K., ADIBI B.
 
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Abstract: 
Fraser or cryptophthalmos syndrome is a rare autosomal recessive disorder characterized by major features such as cryptophthalmos, syndactyly, and abnormal genitalia. Consanguinity is reported in 15 – 24.8% of the cases. The diagnosis of this syndrome can be made on clinical examination; therefore we present the clinical findings of a rare case of Fraser syndrome in a female infant.
 
Keyword(s): CRYPTOPHTHALMOS SYNDROME • CRYPTOPHTHALMOS-SYNDACTYLY SYNDROME • FRASER SYNDROME
 
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