Literature DB >> 25590398

Congenital abnormalities of the posterior fossa.

Thangamadhan Bosemani1, Gunes Orman, Eugen Boltshauser, Aylin Tekes, Thierry A G M Huisman, Andrea Poretti.   

Abstract

The frequency and importance of the evaluation of the posterior fossa have increased significantly over the past 20 years owing to advances in neuroimaging. Nowadays, conventional and advanced neuroimaging techniques allow detailed evaluation of the complex anatomic structures within the posterior fossa. A wide spectrum of congenital abnormalities has been demonstrated, including malformations (anomalies due to an alteration of the primary developmental program caused by a genetic defect) and disruptions (anomalies due to the breakdown of a structure that had a normal developmental potential). Familiarity with the spectrum of congenital posterior fossa anomalies and their well-defined diagnostic criteria is crucial for optimal therapy, an accurate prognosis, and correct genetic counseling. The authors discuss the spectrum of posterior fossa malformations and disruptions, with emphasis on neuroimaging findings (including diagnostic criteria), neurologic presentation, systemic involvement, prognosis, and risk of recurrence. RSNA, 2015

Entities:  

Mesh:

Year:  2015        PMID: 25590398     DOI: 10.1148/rg.351140038

Source DB:  PubMed          Journal:  Radiographics        ISSN: 0271-5333            Impact factor:   5.333


  25 in total

1.  Cerebellar Bottom-of-Fissure Dysplasia-a Novel Cerebellar Gray Matter Neuroimaging Pattern.

Authors:  Andrea Poretti; Andrea Capone; Anette Hackenberg; Ingeborg Kraegeloh-Mann; Gerhard Kurlemann; Guido Laube; Joachim Pietz; Mareike Schimmel; Wolfram Schwindt; Ianina Scheer; Eugen Boltshauser
Journal:  Cerebellum       Date:  2016-12       Impact factor: 3.847

2.  Diagnosis of Joubert syndrome via ultrasonography.

Authors:  Baris Buke; Emre Canverenler; Göksun İpek; Semiha Canverenler; Hatice Akkaya
Journal:  J Med Ultrason (2001)       Date:  2016-10-26       Impact factor: 1.314

3.  Dandy-Walker malformation and syringomyelia: a rare association.

Authors:  Valentina Baro; Renzo Manara; Luca Denaro; Domenico d'Avella
Journal:  Childs Nerv Syst       Date:  2018-03-12       Impact factor: 1.475

4.  Blake's pouch cyst in children: Atypical clinical presentation.

Authors:  Martina Bontognali; Andrea Poretti; Raphael Guzman; Thierry Agm Huisman; Gian Paolo Ramelli
Journal:  Neuroradiol J       Date:  2017-06-27

Review 5.  Magnetic resonance imaging of the brainstem in children, part 1: imaging techniques, embryology, anatomy and review of congenital conditions.

Authors:  Asha Sarma; Josh M Heck; Josephine Ndolo; Allen Newton; Sumit Pruthi
Journal:  Pediatr Radiol       Date:  2021-01-26

6.  Expanding the spectrum of congenital anomalies of the diencephalic-mesencephalic junction.

Authors:  Mariasavina Severino; Domenico Tortora; Angela Pistorio; Luca Antonio Ramenghi; Flavia Napoli; Maria Margherita Mancardi; Pasquale Striano; Valeria Capra; Andrea Rossi
Journal:  Neuroradiology       Date:  2015-10-07       Impact factor: 2.804

7.  Tubulin-related cerebellar dysplasia: definition of a distinct pattern of cerebellar malformation.

Authors:  Romina Romaniello; Filippo Arrigoni; Elena Panzeri; Andrea Poretti; Alessia Micalizzi; Andrea Citterio; Maria Francesca Bedeschi; Angela Berardinelli; Raffaella Cusmai; Stefano D'Arrigo; Alessandro Ferraris; Annette Hackenberg; Alma Kuechler; Margherita Mancardi; Sara Nuovo; Barbara Oehl-Jaschkowitz; Andrea Rossi; Sabrina Signorini; Frank Tüttelmann; Dagmar Wahl; Ute Hehr; Eugen Boltshauser; Maria Teresa Bassi; Enza Maria Valente; Renato Borgatti
Journal:  Eur Radiol       Date:  2017-07-04       Impact factor: 5.315

8.  Anatomic Variability of the Morphometric Parameters of the Fourth Ventricle of the Brain.

Authors:  Iuliia Zhuravlova; Maryna Kornieieva; Erik Rodrigues
Journal:  J Neurol Surg B Skull Base       Date:  2017-09-11

9.  A novel COL4A1 variant associated with recurrent epistaxis and glioblastoma.

Authors:  Kohei Muto; Ryosuke Miyamoto; Yuka Terasawa; Yoshimitsu Shimatani; Keijiro Hara; Takumi Kakimoto; Tatsuya Fukumoto; Yusuke Osaki; Koji Fujita; Masafumi Harada; Hisanori Uehara; Yasushi Takagi; Yuishin Izumi
Journal:  Hum Genome Var       Date:  2021-05-14

10.  Clinical, neuroradiological and molecular characterization of cerebellar dysplasia with cysts (Poretti-Boltshauser syndrome).

Authors:  Alessia Micalizzi; Andrea Poretti; Marta Romani; Monia Ginevrino; Tommaso Mazza; Chiara Aiello; Ginevra Zanni; Bastian Baumgartner; Renato Borgatti; Knut Brockmann; Ana Camacho; Gaetano Cantalupo; Martin Haeusler; Christiane Hikel; Andrea Klein; Giorgia Mandrile; Eugenio Mercuri; Dietz Rating; Romina Romaniello; Filippo Maria Santorelli; Mareike Schimmel; Luigina Spaccini; Serap Teber; Arpad von Moers; Sarah Wente; Andreas Ziegler; Andrea Zonta; Enrico Bertini; Eugen Boltshauser; Enza Maria Valente
Journal:  Eur J Hum Genet       Date:  2016-03-02       Impact factor: 4.246

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.