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A Unique Presentation of Amniotic Band Syndrome: A Newborn With a Tail

A 1-day-old late preterm, small-for-gestational-age female presented with a caudal appendage—a rare finding—and abnormalities in all 4 limbs most consistent with amniotic band syndrome. The caudal appendage was lateral to midline, measured 3 cm × 0.5 cm, and had no bony abnormalities or spinal cord...

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Detalles Bibliográficos
Autores principales: Brown, Carla, Baber, Megan, White, Gwenevere
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9513563/
https://www.ncbi.nlm.nih.gov/pubmed/36176488
http://dx.doi.org/10.1177/2333794X221127545
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author Brown, Carla
Baber, Megan
White, Gwenevere
author_facet Brown, Carla
Baber, Megan
White, Gwenevere
author_sort Brown, Carla
collection PubMed
description A 1-day-old late preterm, small-for-gestational-age female presented with a caudal appendage—a rare finding—and abnormalities in all 4 limbs most consistent with amniotic band syndrome. The caudal appendage was lateral to midline, measured 3 cm × 0.5 cm, and had no bony abnormalities or spinal cord tethering. Limb abnormalities consisted of brachydactyly, oligodactyly, and syndactyly. Renal and head ultrasounds and an echocardiogram were normal. Chromosomal microarray showed deletion of EPHA3, which is not associated with a known phenotype. The multidisciplinary approach of managing this infant with the rare finding of a caudal appendage and limb abnormalities is presented.
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spelling pubmed-95135632022-09-28 A Unique Presentation of Amniotic Band Syndrome: A Newborn With a Tail Brown, Carla Baber, Megan White, Gwenevere Glob Pediatr Health Case Report A 1-day-old late preterm, small-for-gestational-age female presented with a caudal appendage—a rare finding—and abnormalities in all 4 limbs most consistent with amniotic band syndrome. The caudal appendage was lateral to midline, measured 3 cm × 0.5 cm, and had no bony abnormalities or spinal cord tethering. Limb abnormalities consisted of brachydactyly, oligodactyly, and syndactyly. Renal and head ultrasounds and an echocardiogram were normal. Chromosomal microarray showed deletion of EPHA3, which is not associated with a known phenotype. The multidisciplinary approach of managing this infant with the rare finding of a caudal appendage and limb abnormalities is presented. SAGE Publications 2022-09-24 /pmc/articles/PMC9513563/ /pubmed/36176488 http://dx.doi.org/10.1177/2333794X221127545 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page(https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Case Report
Brown, Carla
Baber, Megan
White, Gwenevere
A Unique Presentation of Amniotic Band Syndrome: A Newborn With a Tail
title A Unique Presentation of Amniotic Band Syndrome: A Newborn With a Tail
title_full A Unique Presentation of Amniotic Band Syndrome: A Newborn With a Tail
title_fullStr A Unique Presentation of Amniotic Band Syndrome: A Newborn With a Tail
title_full_unstemmed A Unique Presentation of Amniotic Band Syndrome: A Newborn With a Tail
title_short A Unique Presentation of Amniotic Band Syndrome: A Newborn With a Tail
title_sort unique presentation of amniotic band syndrome: a newborn with a tail
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9513563/
https://www.ncbi.nlm.nih.gov/pubmed/36176488
http://dx.doi.org/10.1177/2333794X221127545
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