Cargando…
Phocomelia: Case report and differential diagnosis
While rarely seen in the present-day Western world, phocomelia is not uncommon in underdeveloped countries. Phocomelia is an abnormality in which the limbs are not fully formed. It may be inherited as an autosomal recessive or dominant disorder. This case concerns a 12-year-old Afghan boy with multi...
Autor principal: | |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4899934/ https://www.ncbi.nlm.nih.gov/pubmed/27307936 http://dx.doi.org/10.2484/rcr.v6i4.561 |
_version_ | 1782436558140342272 |
---|---|
author | Osadsky, Captain Rasto |
author_facet | Osadsky, Captain Rasto |
author_sort | Osadsky, Captain Rasto |
collection | PubMed |
description | While rarely seen in the present-day Western world, phocomelia is not uncommon in underdeveloped countries. Phocomelia is an abnormality in which the limbs are not fully formed. It may be inherited as an autosomal recessive or dominant disorder. This case concerns a 12-year-old Afghan boy with multiple skeletal anomalies, most prominently of his right arm, including aplasia of the entire proximal humerus, hypoplasia of the clavicle and scapula, and absence of the radial ray and thumb. A hypoplastic left thumb was also present. Other anomalies included thoracic scoliosis, upper thoracic hemivertebrae, and mild cardiomegaly. The differential diagnosis and likely diagnosis are discussed. |
format | Online Article Text |
id | pubmed-4899934 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-48999342016-06-15 Phocomelia: Case report and differential diagnosis Osadsky, Captain Rasto Radiol Case Rep Article While rarely seen in the present-day Western world, phocomelia is not uncommon in underdeveloped countries. Phocomelia is an abnormality in which the limbs are not fully formed. It may be inherited as an autosomal recessive or dominant disorder. This case concerns a 12-year-old Afghan boy with multiple skeletal anomalies, most prominently of his right arm, including aplasia of the entire proximal humerus, hypoplasia of the clavicle and scapula, and absence of the radial ray and thumb. A hypoplastic left thumb was also present. Other anomalies included thoracic scoliosis, upper thoracic hemivertebrae, and mild cardiomegaly. The differential diagnosis and likely diagnosis are discussed. Elsevier 2015-11-06 /pmc/articles/PMC4899934/ /pubmed/27307936 http://dx.doi.org/10.2484/rcr.v6i4.561 Text en © 2011 The Authors. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Osadsky, Captain Rasto Phocomelia: Case report and differential diagnosis |
title | Phocomelia: Case report and differential diagnosis |
title_full | Phocomelia: Case report and differential diagnosis |
title_fullStr | Phocomelia: Case report and differential diagnosis |
title_full_unstemmed | Phocomelia: Case report and differential diagnosis |
title_short | Phocomelia: Case report and differential diagnosis |
title_sort | phocomelia: case report and differential diagnosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4899934/ https://www.ncbi.nlm.nih.gov/pubmed/27307936 http://dx.doi.org/10.2484/rcr.v6i4.561 |
work_keys_str_mv | AT osadskycaptainrasto phocomeliacasereportanddifferentialdiagnosis |