Literature DB >> 19289482

Posterior fossa abnormalities in hereditary spastic paraparesis with spastin mutations.

C Scuderi1, M Fichera, G Calabrese, M Elia, C Amato, M Savio, E Borgione, G A Vitello, S A Musumeci.   

Abstract

BACKGROUND: Hereditary spastic paraparesis (HPS) linked to mutations in the spastin gene (SPG4) is considered to be a pure form of spastic hereditary paraparesis. However, in this disease also other signs of central nervous system involvement are frequently found.
METHODS: Clinical, genetical and neuroradiological investigations were carried out in a large family with autosomal dominant spastic paraparesis and in a sporadic case with spastic paraparesis.
RESULTS: Additional clinical and molecular data are provided, studying other members of the same pedigree, as already described, with a five-base deletion in exon 9 of the SPG4 gene (1215-1219delTATAA) whose members show MRI anomalies that fall within the Dandy-Walker continuum. Furthermore, an unrelated female patient with hypoplasia of the cerebellar vermis is indicated, carrying a de novo previously reported mutation of the SPG4 gene (c.1741C>T p.R581X).
CONCLUSIONS: Spastin may play an important role in the development of the central nervous system and in particular in the development of the structures of posterior fossa.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19289482     DOI: 10.1136/jnnp.2008.154807

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN: 0022-3050            Impact factor:   10.154


  4 in total

1.  Gray and white matter alterations in hereditary spastic paraplegia type SPG4 and clinical correlations.

Authors:  Tobias Lindig; Benjamin Bender; Till-Karsten Hauser; Sarah Mang; Daniel Schweikardt; Uwe Klose; Kathrin N Karle; Rebecca Schüle; Ludger Schöls; Tim W Rattay
Journal:  J Neurol       Date:  2015-06-09       Impact factor: 4.849

2.  Mutational spectrum of the SPG4 (SPAST) and SPG3A (ATL1) genes in Spanish patients with hereditary spastic paraplegia.

Authors:  Victoria Alvarez; Elena Sánchez-Ferrero; Christian Beetz; Marta Díaz; Belén Alonso; Ana I Corao; Josep Gámez; Jesús Esteban; Juan F Gonzalo; Samuel I Pascual-Pascual; Adolfo López de Munain; Germán Moris; Renne Ribacoba; Celedonio Márquez; Jordi Rosell; Rosario Marín; Maria J García-Barcina; Emilia Del Castillo; Carmen Benito; Eliecer Coto
Journal:  BMC Neurol       Date:  2010-10-08       Impact factor: 2.474

Review 3.  Neuroimaging in Hereditary Spastic Paraplegias: Current Use and Future Perspectives.

Authors:  Felipe Franco da Graça; Thiago Junqueira Ribeiro de Rezende; Luiz Felipe Rocha Vasconcellos; José Luiz Pedroso; Orlando Graziani P Barsottini; Marcondes C França
Journal:  Front Neurol       Date:  2019-01-16       Impact factor: 4.003

4.  Clinical-Genetic Features Influencing Disability in Spastic Paraplegia Type 4: A Cross-sectional Study by the Italian DAISY Network.

Authors:  Salvatore Rossi; Anna Rubegni; Vittorio Riso; Melissa Barghigiani; Maria Teresa Bassi; Roberta Battini; Enrico Bertini; Cristina Cereda; Ettore Cioffi; Chiara Criscuolo; Beatrice Dal Fabbro; Clemente Dato; Maria Grazia D'Angelo; Antonio Di Muzio; Luca Diamanti; Maria Teresa Dotti; Alessandro Filla; Valeria Gioiosa; Rocco Liguori; Andrea Martinuzzi; Roberto Massa; Andrea Mignarri; Rossana Moroni; Olimpia Musumeci; Francesco Nicita; Ilaria Orologio; Laura Orsi; Elena Pegoraro; Antonio Petrucci; Massimo Plumari; Ivana Ricca; Giovanni Rizzo; Silvia Romano; Roberto Rumore; Simone Sampaolo; Marina Scarlato; Marco Seri; Cristina Stefan; Giulia Straccia; Alessandra Tessa; Lorena Travaglini; Rosanna Trovato; Lucia Ulgheri; Giovanni Vazza; Antonio Orlacchio; Gabriella Silvestri; Filippo Maria Santorelli; Mariarosa Anna Beatrice Melone; Carlo Casali
Journal:  Neurol Genet       Date:  2022-03-30
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.