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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
 
 
References: 
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Citations: 
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+ Click to Cite.
APA: Copy

KHOURY, E., & GOL ALIPOUR, M., & HAIDARY, K., & ADIBI, B. (2004). FRASER OR CRYPTOPHTHALMOS SYNDROME:A CASE REPORT. ARCHIVES OF IRANIAN MEDICINE, 7(4), 307-309. https://www.sid.ir/en/journal/ViewPaper.aspx?id=13644



Vancouver: Copy

KHOURY E., GOL ALIPOUR M.J., HAIDARY K., ADIBI B.. FRASER OR CRYPTOPHTHALMOS SYNDROME:A CASE REPORT. ARCHIVES OF IRANIAN MEDICINE. 2004 [cited 2021June17];7(4):307-309. Available from: https://www.sid.ir/en/journal/ViewPaper.aspx?id=13644



IEEE: Copy

KHOURY, E., GOL ALIPOUR, M., HAIDARY, K., ADIBI, B., 2004. FRASER OR CRYPTOPHTHALMOS SYNDROME:A CASE REPORT. ARCHIVES OF IRANIAN MEDICINE, [online] 7(4), pp.307-309. Available: https://www.sid.ir/en/journal/ViewPaper.aspx?id=13644.



 
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