A RARE CASE REPORT OF SIRENOMELIA, THE MERMAID SYNDROME

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SADEGHIPOUR ROUDSARI S.; ABOTORABI SH.S.; FARZAM S.A.

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Journal: Iranian Journal of Surgery Year:2012 | Volume:20 | Issue:1 Page(s): 0-0

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Information Journal Paper

Title

A RARE CASE REPORT OF SIRENOMELIA, THE MERMAID SYNDROME

Author(s)

SADEGHIPOUR ROUDSARI S. | ABOTORABI SH.S. | FARZAM S.A. | Issue Writer Certificate

Keywords

SIRENOMELIAQ3

MERMAID SYNDROMEQ3

CAUDAL REGRESSION SYNDROMEQ3

Abstract

SIRENOMELIA, the MERMAID SYNDROME is an extremely rare and lethal congenital anomaly with an incidence of one in 60.000 to 100.000 pregnancies. It is characterized by complete fusion of the lower limbs associated with external genitalia absence, renal agenesis and anorectal defects. SIRENOMELIA represents the most severe of CAUDAL REGRESSION SYNDROME. Although prenatal diagnosis has been reported even as early as the first trimester, we present an infant delivered from a 19 - year- old primigravida at 33 week's gestation, with a dysmorphic lower limb, agenesis of external urogenital and anorectol atresia. X- Ray (baby gram) and autopsy revealed other anomalies in the infant.The early detection of this syndrome during the first or the second trimester, helps us in the diagnosis of this rare anomaly and in terminating the pregnancy in a less traumatic period.

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APA: Copy

SADEGHIPOUR ROUDSARI, S., ABOTORABI, SH.S., & FARZAM, S.A.. (2012). A RARE CASE REPORT OF SIRENOMELIA, THE MERMAID SYNDROME. IRANIAN JOURNAL OF SURGERY, 20(1), 0-0. SID. https://sid.ir/paper/400133/en

Vancouver: Copy

SADEGHIPOUR ROUDSARI S., ABOTORABI SH.S., FARZAM S.A.. A RARE CASE REPORT OF SIRENOMELIA, THE MERMAID SYNDROME. IRANIAN JOURNAL OF SURGERY[Internet]. 2012;20(1):0-0. Available from: https://sid.ir/paper/400133/en

IEEE: Copy

S. SADEGHIPOUR ROUDSARI, SH.S. ABOTORABI, and S.A. FARZAM, “A RARE CASE REPORT OF SIRENOMELIA, THE MERMAID SYNDROME,” IRANIAN JOURNAL OF SURGERY, vol. 20, no. 1, pp. 0–0, 2012, [Online]. Available: https://sid.ir/paper/400133/en

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