A rare case report of sirenomelia following intracytoplasmic sperm injection embryo transfer
Sirenomelia is a very rare developmental abnormality which is characterized by fusion of lower limb to form a single limb. This condition is often associated with internal organ abnormality and is considered incompatible with life. Sirenomelia is sporadically reported from across the world, but no c...
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Published in: | Journal of human reproductive sciences Vol. 13; no. 1; pp. 71 - 74 |
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Main Authors: | , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Mumbai
Wolters Kluwer India Pvt. Ltd
01-01-2020
Medknow Publications & Media Pvt. Ltd Wolters Kluwer - Medknow |
Subjects: | |
Online Access: | Get full text |
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Summary: | Sirenomelia is a very rare developmental abnormality which is characterized by fusion of lower limb to form a single limb. This condition is often associated with internal organ abnormality and is considered incompatible with life. Sirenomelia is sporadically reported from across the world, but no case associated with artificial reproductive technology (ART) has not been reported. We report a case of sirenomelia in a 29-year old woman who conceived by ART, which to our knowledge is the first reported case in ART. The defect was detected early during first trimester and the pregnancy was terminated. |
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ISSN: | 0974-1208 1998-4766 |
DOI: | 10.4103/jhrs.JHRS_128_19 |