Cargando…

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....

Descripción completa

Detalles Bibliográficos
Autores principales: Dehdashtian, Amir, Dehdashtian, Masoud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications, Pavia, Italy 2016
Materias:
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
_version_ 1782441227194466304
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