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A Male with Cooccurrence of Down Syndrome and Fragile X Syndrome

Down syndrome is the most common identifiable genetic cause of intellectual disability, with a unique physical gestalt that makes diagnosis possible during the newborn period. However, the physical characteristics of Fragile X syndrome are fairly subtle, resulting in the first clinical suspicion oft...

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Detalles Bibliográficos
Autores principales: Anderson, Tovi, Buterbaugh, Allison, Love, Kaitlin, Visootsak, Jeannie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3780622/
https://www.ncbi.nlm.nih.gov/pubmed/24083039
http://dx.doi.org/10.1155/2013/504695
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author Anderson, Tovi
Buterbaugh, Allison
Love, Kaitlin
Visootsak, Jeannie
author_facet Anderson, Tovi
Buterbaugh, Allison
Love, Kaitlin
Visootsak, Jeannie
author_sort Anderson, Tovi
collection PubMed
description Down syndrome is the most common identifiable genetic cause of intellectual disability, with a unique physical gestalt that makes diagnosis possible during the newborn period. However, the physical characteristics of Fragile X syndrome are fairly subtle, resulting in the first clinical suspicion often arising from delayed developmental milestones. In addition, maladaptive behavior and autistic-like tendencies, such as hand flapping, poor eye contact, and hand biting, may be noted in Fragile X syndrome but are not as commonly observed in Down syndrome. Recognition of a potential secondary diagnosis, such as Fragile X syndrome, in individuals with Down syndrome is critical because there have been advances in targeted pharmacologic treatments for both conditions. Thus, an accurate diagnosis has implications in improving the individual's quality of life.
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spelling pubmed-37806222013-09-30 A Male with Cooccurrence of Down Syndrome and Fragile X Syndrome Anderson, Tovi Buterbaugh, Allison Love, Kaitlin Visootsak, Jeannie Case Rep Genet Case Report Down syndrome is the most common identifiable genetic cause of intellectual disability, with a unique physical gestalt that makes diagnosis possible during the newborn period. However, the physical characteristics of Fragile X syndrome are fairly subtle, resulting in the first clinical suspicion often arising from delayed developmental milestones. In addition, maladaptive behavior and autistic-like tendencies, such as hand flapping, poor eye contact, and hand biting, may be noted in Fragile X syndrome but are not as commonly observed in Down syndrome. Recognition of a potential secondary diagnosis, such as Fragile X syndrome, in individuals with Down syndrome is critical because there have been advances in targeted pharmacologic treatments for both conditions. Thus, an accurate diagnosis has implications in improving the individual's quality of life. Hindawi Publishing Corporation 2013 2013-09-12 /pmc/articles/PMC3780622/ /pubmed/24083039 http://dx.doi.org/10.1155/2013/504695 Text en Copyright © 2013 Tovi Anderson et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Anderson, Tovi
Buterbaugh, Allison
Love, Kaitlin
Visootsak, Jeannie
A Male with Cooccurrence of Down Syndrome and Fragile X Syndrome
title A Male with Cooccurrence of Down Syndrome and Fragile X Syndrome
title_full A Male with Cooccurrence of Down Syndrome and Fragile X Syndrome
title_fullStr A Male with Cooccurrence of Down Syndrome and Fragile X Syndrome
title_full_unstemmed A Male with Cooccurrence of Down Syndrome and Fragile X Syndrome
title_short A Male with Cooccurrence of Down Syndrome and Fragile X Syndrome
title_sort male with cooccurrence of down syndrome and fragile x syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3780622/
https://www.ncbi.nlm.nih.gov/pubmed/24083039
http://dx.doi.org/10.1155/2013/504695
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