Literature DB >> 15596767

Hereditary spastic paraplegia with frontal lobe dysfunction: a clinicopathologic study.

D Yanase1, K Komai, T Hamaguchi, S Okino, H Yokoji, T Makifuchi, H Takano, M Yamada.   

Abstract

The authors report an unusual family with hereditary spastic paraplegia (HSP) with frontal lobe dysfunction having the onset in the sixth decade. All the patients showed hypoperfusion in the frontal lobes and thalami on SPECT. Neuropathologic findings revealed thin corpus callosum and degeneration in the thalamic dorsomedial nuclei as well as degeneration of the corticospinal tracts. This family was likely affected by a novel form of HSP characterized by frontal lobe dysfunction caused by thalamic degeneration.

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Year:  2004        PMID: 15596767     DOI: 10.1212/01.wnl.0000145670.15559.b8

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  6 in total

1.  Mania associated with complicated hereditary spastic paraparesis.

Authors:  Raghavendra B Nayak; Govind S Bhogale; Nanasaheb M Patil; Aditya A Pandurangi
Journal:  J Neurosci Rural Pract       Date:  2011-07

2.  Dysfunction of spatacsin leads to axonal pathology in SPG11-linked hereditary spastic paraplegia.

Authors:  Francesc Pérez-Brangulí; Himanshu K Mishra; Iryna Prots; Steven Havlicek; Zacharias Kohl; Domenica Saul; Christine Rummel; Jonatan Dorca-Arevalo; Martin Regensburger; Daniela Graef; Elisabeth Sock; Juan Blasi; Teja W Groemer; Ursula Schlötzer-Schrehardt; Jürgen Winkler; Beate Winner
Journal:  Hum Mol Genet       Date:  2014-05-02       Impact factor: 6.150

3.  Truncating mutations in SPAST patients are associated with a high rate of psychiatric comorbidities in hereditary spastic paraplegia.

Authors:  Viorica Chelban; Arianna Tucci; David S Lynch; James M Polke; Liana Santos; Hallgeir Jonvik; Stanislav Groppa; Nicholas W Wood; Henry Houlden
Journal:  J Neurol Neurosurg Psychiatry       Date:  2017-06-01       Impact factor: 10.154

4.  Spastic Paraplegia Accompanied by Extrapyramidal Sign and Frontal Cognitive Dysfunction.

Authors:  Ryo Sasaki; Yasuyuki Ohta; Kota Sato; Koh Tadokoro; Yoshiaki Takahashi; Jingwei Shang; Mami Takemoto; Nozomi Hishikawa; Toru Yamashita; Hiroyuki Ishiura; Shoji Tsuji; Koji Abe
Journal:  Intern Med       Date:  2019-07-10       Impact factor: 1.271

5.  SPG15 protein deficits are at the crossroads between lysosomal abnormalities, altered lipid metabolism and synaptic dysfunction.

Authors:  Lara Marrone; Paolo M Marchi; Christopher P Webster; Raffaele Marroccella; Ian Coldicott; Steven Reynolds; João Alves-Cruzeiro; Zih-Liang Yang; Adrian Higginbottom; Mukhran Khundadze; Pamela J Shaw; Christian A Hübner; Matthew R Livesey; Mimoun Azzouz
Journal:  Hum Mol Genet       Date:  2022-08-23       Impact factor: 5.121

6.  Cortical Damage Associated With Cognitive and Motor Impairment in Hereditary Spastic Paraplegia: Evidence of a Novel SPAST Mutation.

Authors:  Jian-Zhong Lin; Hong-Hua Zheng; Qi-Lin Ma; Chen Wang; Li-Ping Fan; Han-Ming Wu; Dan-Ni Wang; Jia-Xing Zhang; Yi-Hong Zhan
Journal:  Front Neurol       Date:  2020-05-27       Impact factor: 4.003

  6 in total

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