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Adams-Oliver Syndrome: A Case with Full Expression
Adams-Oliver syndrome (AOS) is characterized by the combination of congenital scalp defects (aplasia cutis congenita) and terminal transverse limb defects of variable severity. It is believed that Adams-Oliver syndrome without major organ abnormalities does not necessarily alter the normal lifespan....
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PAGEPress Publications, Pavia, Italy
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4933813/ https://www.ncbi.nlm.nih.gov/pubmed/27433307 http://dx.doi.org/10.4081/pr.2016.6517 |
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author | Dehdashtian, Amir Dehdashtian, Masoud |
author_facet | Dehdashtian, Amir Dehdashtian, Masoud |
author_sort | Dehdashtian, Amir |
collection | PubMed |
description | Adams-Oliver syndrome (AOS) is characterized by the combination of congenital scalp defects (aplasia cutis congenita) and terminal transverse limb defects of variable severity. It is believed that Adams-Oliver syndrome without major organ abnormalities does not necessarily alter the normal lifespan. We present a case without detectable major organ abnormality contrary to life but with poor weight gain. A male infant with scalp and skin cutis aplasia, generalized cutis aplasia, dilated veins over scalp and trunk, hypoplastic toes and nails of feet, glaucoma, poor feeding and poor weight gain. This report shows a case of AOS without major multiple organ abnormalities but with poor feeding and abnormal weight gain that may be alter the normal lifespan. |
format | Online Article Text |
id | pubmed-4933813 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | PAGEPress Publications, Pavia, Italy |
record_format | MEDLINE/PubMed |
spelling | pubmed-49338132016-07-18 Adams-Oliver Syndrome: A Case with Full Expression Dehdashtian, Amir Dehdashtian, Masoud Pediatr Rep Case Report Adams-Oliver syndrome (AOS) is characterized by the combination of congenital scalp defects (aplasia cutis congenita) and terminal transverse limb defects of variable severity. It is believed that Adams-Oliver syndrome without major organ abnormalities does not necessarily alter the normal lifespan. We present a case without detectable major organ abnormality contrary to life but with poor weight gain. A male infant with scalp and skin cutis aplasia, generalized cutis aplasia, dilated veins over scalp and trunk, hypoplastic toes and nails of feet, glaucoma, poor feeding and poor weight gain. This report shows a case of AOS without major multiple organ abnormalities but with poor feeding and abnormal weight gain that may be alter the normal lifespan. PAGEPress Publications, Pavia, Italy 2016-06-27 /pmc/articles/PMC4933813/ /pubmed/27433307 http://dx.doi.org/10.4081/pr.2016.6517 Text en ©Copyright A. Dehdashtian and M. Dehdashtian http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Dehdashtian, Amir Dehdashtian, Masoud Adams-Oliver Syndrome: A Case with Full Expression |
title | Adams-Oliver Syndrome: A Case with Full Expression |
title_full | Adams-Oliver Syndrome: A Case with Full Expression |
title_fullStr | Adams-Oliver Syndrome: A Case with Full Expression |
title_full_unstemmed | Adams-Oliver Syndrome: A Case with Full Expression |
title_short | Adams-Oliver Syndrome: A Case with Full Expression |
title_sort | adams-oliver syndrome: a case with full expression |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4933813/ https://www.ncbi.nlm.nih.gov/pubmed/27433307 http://dx.doi.org/10.4081/pr.2016.6517 |
work_keys_str_mv | AT dehdashtianamir adamsoliversyndromeacasewithfullexpression AT dehdashtianmasoud adamsoliversyndromeacasewithfullexpression |