Longitudinal neurocognitive outcome in an adolescent with Hurler-Scheie syndrome

An adolescent with Hurler-Scheie syndrome is reported. This now 15 year-old-young woman was initially diagnosed at age 4. She was assessed for neurocognitive functioning at ages 5, 13, and 15 years. Results show a significant decline in intellectual functioning from the superior range to the average...

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Autores principales: Elkin, T David, Megason, Gail, Robinson, Anita, Bock, Hans-Georg O, Schrimsher, Gregory, Muenzer, Joseph
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2006
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2671818/
https://www.ncbi.nlm.nih.gov/pubmed/19412486
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author Elkin, T David
Megason, Gail
Robinson, Anita
Bock, Hans-Georg O
Schrimsher, Gregory
Muenzer, Joseph
author_facet Elkin, T David
Megason, Gail
Robinson, Anita
Bock, Hans-Georg O
Schrimsher, Gregory
Muenzer, Joseph
author_sort Elkin, T David
collection PubMed
description An adolescent with Hurler-Scheie syndrome is reported. This now 15 year-old-young woman was initially diagnosed at age 4. She was assessed for neurocognitive functioning at ages 5, 13, and 15 years. Results show a significant decline in intellectual functioning from the superior range to the average range from age 5 to age 13, and then no change from age 13 to age 15. The relationship between Hurler-Scheie syndrome, premorbid intellectual functioning, and cognitive–behavioral interventions are discussed in light of the longitudinal neurocognitive effects of this disease.
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spelling pubmed-26718182009-04-30 Longitudinal neurocognitive outcome in an adolescent with Hurler-Scheie syndrome Elkin, T David Megason, Gail Robinson, Anita Bock, Hans-Georg O Schrimsher, Gregory Muenzer, Joseph Neuropsychiatr Dis Treat Case Reports An adolescent with Hurler-Scheie syndrome is reported. This now 15 year-old-young woman was initially diagnosed at age 4. She was assessed for neurocognitive functioning at ages 5, 13, and 15 years. Results show a significant decline in intellectual functioning from the superior range to the average range from age 5 to age 13, and then no change from age 13 to age 15. The relationship between Hurler-Scheie syndrome, premorbid intellectual functioning, and cognitive–behavioral interventions are discussed in light of the longitudinal neurocognitive effects of this disease. Dove Medical Press 2006-09 /pmc/articles/PMC2671818/ /pubmed/19412486 Text en © 2006 Dove Medical Press Limited. All rights reserved
spellingShingle Case Reports
Elkin, T David
Megason, Gail
Robinson, Anita
Bock, Hans-Georg O
Schrimsher, Gregory
Muenzer, Joseph
Longitudinal neurocognitive outcome in an adolescent with Hurler-Scheie syndrome
title Longitudinal neurocognitive outcome in an adolescent with Hurler-Scheie syndrome
title_full Longitudinal neurocognitive outcome in an adolescent with Hurler-Scheie syndrome
title_fullStr Longitudinal neurocognitive outcome in an adolescent with Hurler-Scheie syndrome
title_full_unstemmed Longitudinal neurocognitive outcome in an adolescent with Hurler-Scheie syndrome
title_short Longitudinal neurocognitive outcome in an adolescent with Hurler-Scheie syndrome
title_sort longitudinal neurocognitive outcome in an adolescent with hurler-scheie syndrome
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2671818/
https://www.ncbi.nlm.nih.gov/pubmed/19412486
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