Literature DB >> 21561552

Imaging and clinical features in a child with Loeys-Dietz syndrome. A case report.

B Suarez1, A Caldera, M Castillo.   

Abstract

We describe a boy with Loeys-Dietz syndrome (LDS) a genetic and recently described condition that affects connective tissues belonging to a group of Marfan-related disorders. Since there are only a few cases reported misdiagnosis may not be uncommon. Radiological findings in our patient include pectus excavatum, aortic root dilatation, diffuse dilatation of the intracerebral vessels and a Chiari I malformation. We describe the imaging findings, clinical presentation and diagnosis criteria of this entity.

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Year:  2011        PMID: 21561552      PMCID: PMC3278033          DOI: 10.1177/159101991101700102

Source DB:  PubMed          Journal:  Interv Neuroradiol        ISSN: 1591-0199            Impact factor:   1.610


  9 in total

Review 1.  Loeys-Dietz syndrome: MDCT angiography findings.

Authors:  Pamela T Johnson; Jennifer K Chen; Bart L Loeys; Harry C Dietz; Elliot K Fishman
Journal:  AJR Am J Roentgenol       Date:  2007-07       Impact factor: 3.959

2.  Loeys-Dietz syndrome: a Marfan-like syndrome associated with aggressive vasculopathy.

Authors:  J T L Choo; T H Tan; A H M Lai; K Y Wong
Journal:  Singapore Med J       Date:  2009-10       Impact factor: 1.858

Review 3.  The Loeys-Dietz syndrome: an update for the clinician.

Authors:  Christine Van Hemelrijk; Marjolijn Renard; Bart Loeys
Journal:  Curr Opin Cardiol       Date:  2010-11       Impact factor: 2.161

4.  High prevalence of vertebral artery tortuosity of Loeys-Dietz syndrome in comparison with Marfan syndrome.

Authors:  Atsushi K Kono; Masahiro Higashi; Hiroko Morisaki; Takayuki Morisaki; Yoshiaki Tsutsumi; Koichi Akutsu; Hiroaki Naito; Kazuro Sugimura
Journal:  Jpn J Radiol       Date:  2010-05-29       Impact factor: 2.374

5.  Importance of the clinical recognition of Loeys-Dietz syndrome in the neonatal period.

Authors:  Anji T Yetman; Rebecca S Beroukhim; Dunbar D Ivy; David Manchester
Journal:  Pediatrics       Date:  2007-05       Impact factor: 7.124

6.  Loeys-Dietz syndrome type I and type II: clinical findings and novel mutations in two Italian patients.

Authors:  Bruno Drera; Marco Ritelli; Nicoletta Zoppi; Anita Wischmeijer; Maria Gnoli; Rossella Fattori; Pier Giacomo Calzavara-Pinton; Sergio Barlati; Marina Colombi
Journal:  Orphanet J Rare Dis       Date:  2009-11-02       Impact factor: 4.123

Review 7.  A new sporadic case of early-onset Loeys-Dietz syndrome due to the recurrent mutation p.R528C in the TGFBR2 gene substantiates interindividual clinical variability.

Authors:  A Jamsheer; C Henggeler; J Wierzba; B Loeys; A De Paepe; Ch Stheneur; N Badziag; K Matuszewska; G Matyas; A Latos-Bielenska
Journal:  J Appl Genet       Date:  2009       Impact factor: 3.240

8.  A Japanese family of typical Loeys-Dietz syndrome with a TGFBR2 mutation.

Authors:  Yosuke Togashi; Hiroto Sakoda; Akira Nishimura; Naomichi Matsumoto; Hisatoyo Hiraoka; Yuji Matsuzawa
Journal:  Intern Med       Date:  2007-12-17       Impact factor: 1.271

9.  Neuroradiologic manifestations of Loeys-Dietz syndrome type 1.

Authors:  V J Rodrigues; S Elsayed; B L Loeys; H C Dietz; D M Yousem
Journal:  AJNR Am J Neuroradiol       Date:  2009-06-25       Impact factor: 3.825

  9 in total

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