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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...

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Autores principales: Velasquez Restrespo, Sara, Oboli, Victor N, Kumar, Dyuti, Marino-Villamizar, Catalina, Khanna, Shefali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
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.
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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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