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Ulnar Longitudinal Deficiency: A Case Report
Ulnar longitudinal deficiency (ULD) is a rare skeletal condition marked by the partial or complete failure of the formation of the ulna. This rare condition is often associated with fixed flexion deformity, radial head subluxation, complex carpal, metacarpal, and digital abnormalities. Most presenta...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10256245/ https://www.ncbi.nlm.nih.gov/pubmed/37304382 http://dx.doi.org/10.7759/cureus.40111 |
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author | Velasquez Restrespo, Sara Oboli, Victor N Kumar, Dyuti Marino-Villamizar, Catalina Khanna, Shefali |
author_facet | Velasquez Restrespo, Sara Oboli, Victor N Kumar, Dyuti Marino-Villamizar, Catalina Khanna, Shefali |
author_sort | Velasquez Restrespo, Sara |
collection | PubMed |
description | Ulnar longitudinal deficiency (ULD) is a rare skeletal condition marked by the partial or complete failure of the formation of the ulna. This rare condition is often associated with fixed flexion deformity, radial head subluxation, complex carpal, metacarpal, and digital abnormalities. Most presentations are male-preponderant and right-sided. Different classifications have described ULD. Usually, the condition is not associated with systemic findings; however, detailed physical examination and radiologic evaluations are crucial for assessing and managing affected patients. We report a rare case of ULD in an 11-month-old female infant with congenital absence of the left ulna, four digits, and a postaxial hypoplastic finger. |
format | Online Article Text |
id | pubmed-10256245 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
spelling | pubmed-102562452023-06-10 Ulnar Longitudinal Deficiency: A Case Report Velasquez Restrespo, Sara Oboli, Victor N Kumar, Dyuti Marino-Villamizar, Catalina Khanna, Shefali Cureus Pediatrics Ulnar longitudinal deficiency (ULD) is a rare skeletal condition marked by the partial or complete failure of the formation of the ulna. This rare condition is often associated with fixed flexion deformity, radial head subluxation, complex carpal, metacarpal, and digital abnormalities. Most presentations are male-preponderant and right-sided. Different classifications have described ULD. Usually, the condition is not associated with systemic findings; however, detailed physical examination and radiologic evaluations are crucial for assessing and managing affected patients. We report a rare case of ULD in an 11-month-old female infant with congenital absence of the left ulna, four digits, and a postaxial hypoplastic finger. Cureus 2023-06-08 /pmc/articles/PMC10256245/ /pubmed/37304382 http://dx.doi.org/10.7759/cureus.40111 Text en Copyright © 2023, Velasquez Restrespo et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Pediatrics Velasquez Restrespo, Sara Oboli, Victor N Kumar, Dyuti Marino-Villamizar, Catalina Khanna, Shefali Ulnar Longitudinal Deficiency: A Case Report |
title | Ulnar Longitudinal Deficiency: A Case Report |
title_full | Ulnar Longitudinal Deficiency: A Case Report |
title_fullStr | Ulnar Longitudinal Deficiency: A Case Report |
title_full_unstemmed | Ulnar Longitudinal Deficiency: A Case Report |
title_short | Ulnar Longitudinal Deficiency: A Case Report |
title_sort | ulnar longitudinal deficiency: a case report |
topic | Pediatrics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10256245/ https://www.ncbi.nlm.nih.gov/pubmed/37304382 http://dx.doi.org/10.7759/cureus.40111 |
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