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Mania associated with complicated hereditary spastic paraparesis

Hereditary spastic paraparesis (HSP) is an inherited group of neurological disorders with progressive lower limb spasticity. HSP can be clinically grouped into pure and complicated forms. Pure HSP is one without any associated neurological/psychiatric comorbidity. Depression is the most common psych...

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Autores principales: Nayak, Raghavendra B, Bhogale, Govind S, Patil, Nanasaheb M, Pandurangi, Aditya A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3159362/
https://www.ncbi.nlm.nih.gov/pubmed/21897689
http://dx.doi.org/10.4103/0976-3147.83592
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author Nayak, Raghavendra B
Bhogale, Govind S
Patil, Nanasaheb M
Pandurangi, Aditya A
author_facet Nayak, Raghavendra B
Bhogale, Govind S
Patil, Nanasaheb M
Pandurangi, Aditya A
author_sort Nayak, Raghavendra B
collection PubMed
description Hereditary spastic paraparesis (HSP) is an inherited group of neurological disorders with progressive lower limb spasticity. HSP can be clinically grouped into pure and complicated forms. Pure HSP is one without any associated neurological/psychiatric comorbidity. Depression is the most common psychiatric comorbidity. Presence of mania or bipolar affective illness with HSP is a rare phenomenon. We report a case of a 17-year-old boy who presented with classical features of HSP with complaints of excessive happiness, irritability, increased self-esteem and decreased sleep since 1 month. The patient also had complex partial seizure ever since he had features of HSP. The patient's father and younger sister suffer from pure HSP. The patient was diagnosed to have first episode mania with complicated HSP. The details of treatment and possible neurobiology are discussed in this case report.
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spelling pubmed-31593622011-09-06 Mania associated with complicated hereditary spastic paraparesis Nayak, Raghavendra B Bhogale, Govind S Patil, Nanasaheb M Pandurangi, Aditya A J Neurosci Rural Pract Case Report Hereditary spastic paraparesis (HSP) is an inherited group of neurological disorders with progressive lower limb spasticity. HSP can be clinically grouped into pure and complicated forms. Pure HSP is one without any associated neurological/psychiatric comorbidity. Depression is the most common psychiatric comorbidity. Presence of mania or bipolar affective illness with HSP is a rare phenomenon. We report a case of a 17-year-old boy who presented with classical features of HSP with complaints of excessive happiness, irritability, increased self-esteem and decreased sleep since 1 month. The patient also had complex partial seizure ever since he had features of HSP. The patient's father and younger sister suffer from pure HSP. The patient was diagnosed to have first episode mania with complicated HSP. The details of treatment and possible neurobiology are discussed in this case report. Medknow Publications 2011 /pmc/articles/PMC3159362/ /pubmed/21897689 http://dx.doi.org/10.4103/0976-3147.83592 Text en Copyright: © Journal of Neurosciences in Rural Practice http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Nayak, Raghavendra B
Bhogale, Govind S
Patil, Nanasaheb M
Pandurangi, Aditya A
Mania associated with complicated hereditary spastic paraparesis
title Mania associated with complicated hereditary spastic paraparesis
title_full Mania associated with complicated hereditary spastic paraparesis
title_fullStr Mania associated with complicated hereditary spastic paraparesis
title_full_unstemmed Mania associated with complicated hereditary spastic paraparesis
title_short Mania associated with complicated hereditary spastic paraparesis
title_sort mania associated with complicated hereditary spastic paraparesis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3159362/
https://www.ncbi.nlm.nih.gov/pubmed/21897689
http://dx.doi.org/10.4103/0976-3147.83592
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