Human tail in a newborn
Human tails are extremely infrequent and are generally diagnosed after birth, with no antenatal or family history associated with its occurrence. Different classification systems exist, however given its association with spinal dysraphism, it is important to include imaging studies during the assess...
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Main Authors: | , , , , , , , |
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Format: | Book |
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Elsevier,
2022-01-01T00:00:00Z.
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LEADER | 00000 am a22000003u 4500 | ||
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001 | doaj_543c5f2e5e65404a86d02cbf84fa23d7 | ||
042 | |a dc | ||
100 | 1 | 0 | |a Josue Rueda |e author |
700 | 1 | 0 | |a Jorge Gutierrez |e author |
700 | 1 | 0 | |a Jose Facio |e author |
700 | 1 | 0 | |a Abraham Alarcón |e author |
700 | 1 | 0 | |a Edgar Armijo |e author |
700 | 1 | 0 | |a Daniela Cisneros |e author |
700 | 1 | 0 | |a Susana Hernandez |e author |
700 | 1 | 0 | |a Gerardo Muñoz |e author |
245 | 0 | 0 | |a Human tail in a newborn |
260 | |b Elsevier, |c 2022-01-01T00:00:00Z. | ||
500 | |a 2213-5766 | ||
500 | |a 10.1016/j.epsc.2021.102098 | ||
520 | |a Human tails are extremely infrequent and are generally diagnosed after birth, with no antenatal or family history associated with its occurrence. Different classification systems exist, however given its association with spinal dysraphism, it is important to include imaging studies during the assessment of patients with this congenital anomaly. We present the case of a human tail with no underlying spinal dysraphism that successfully underwent simple resection and reconstruction with Limberg plasty. | ||
546 | |a EN | ||
690 | |a Human tail | ||
690 | |a Vestigial tail | ||
690 | |a Pseudotail | ||
690 | |a Pediatrics | ||
690 | |a RJ1-570 | ||
690 | |a Surgery | ||
690 | |a RD1-811 | ||
655 | 7 | |a article |2 local | |
786 | 0 | |n Journal of Pediatric Surgery Case Reports, Vol 76, Iss , Pp 102098- (2022) | |
787 | 0 | |n http://www.sciencedirect.com/science/article/pii/S2213576621003195 | |
787 | 0 | |n https://doaj.org/toc/2213-5766 | |
856 | 4 | 1 | |u https://doaj.org/article/543c5f2e5e65404a86d02cbf84fa23d7 |z Connect to this object online. |