Literature DB >> 11392528

Seckel's syndrome and malformations of cortical development: report of three new cases and review of the literature.

G Capovilla1, M E Lorenzetti, A Montagnini, R Borgatti, P Piccinelli, L Giordano, P Accorsi, R Caudana.   

Abstract

Seckel's syndrome is a rare form of primordial dwarfism, characterized by peculiar facial appearance. In the past, this condition was overdiagnosed, and most attention was given to the facial and skeletal features to define more precise diagnostic criteria. The presence of mental retardation and neurologic signs is one of the peculiar features of this syndrome, but only recently were rare cases of malformation of cortical development described, as documented by magnetic resonance imaging (MRI). Here, we present three new cases of Seckel's syndrome showing different malformations of cortical development (one gyral hypoplasia, one macrogyria and partial corpus callosum agenesis, and one bilateral opercular macrogyria). We hypothesize that the different types of clinical expression of our patients could be explained by different malformation of cortical development types. We think that MRI studies could be performed in malformative syndromes because of the possible correlations between type and extent of the lesion and the clinical picture of any individual case.

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Year:  2001        PMID: 11392528     DOI: 10.1177/088307380101600516

Source DB:  PubMed          Journal:  J Child Neurol        ISSN: 0883-0738            Impact factor:   1.987


  5 in total

1.  ATR maintains select progenitors during nervous system development.

Authors:  Youngsoo Lee; Erin R P Shull; Pierre-Olivier Frappart; Sachin Katyal; Vanessa Enriquez-Rios; Jingfeng Zhao; Helen R Russell; Eric J Brown; Peter J McKinnon
Journal:  EMBO J       Date:  2012-01-20       Impact factor: 11.598

2.  Seckel syndrome with chromosomal 18 deletion.

Authors:  Inusha Panigrahi; Satvinder Kaur; Ketan Kulkarni; Reena Das; Ram Kumar Marwaha
Journal:  Indian J Pediatr       Date:  2009-12-11       Impact factor: 1.967

3.  Semilobar holoprosencephaly in Seckel syndrome.

Authors:  Rakesh Kumar; Manoj Rawal; Shalini Agarwal; Geeta Gathwala
Journal:  Indian J Pediatr       Date:  2008-06-08       Impact factor: 1.967

4.  Disruption of mouse Cenpj, a regulator of centriole biogenesis, phenocopies Seckel syndrome.

Authors:  Rebecca E McIntyre; Pavithra Lakshminarasimhan Chavali; Ozama Ismail; Damian M Carragher; Gabriela Sanchez-Andrade; Josep V Forment; Beiyuan Fu; Martin Del Castillo Velasco-Herrera; Andrew Edwards; Louise van der Weyden; Fengtang Yang; Ramiro Ramirez-Solis; Jeanne Estabel; Ferdia A Gallagher; Darren W Logan; Mark J Arends; Stephen H Tsang; Vinit B Mahajan; Cheryl L Scudamore; Jacqueline K White; Stephen P Jackson; Fanni Gergely; David J Adams
Journal:  PLoS Genet       Date:  2012-11-15       Impact factor: 5.917

5.  Central nervous system vasculopathy and Seckel syndrome: case illustration and systematic review.

Authors:  Osama Khojah; Saeed Alamoudi; Nouf Aldawsari; Mohammed Babgi; Ahmed Lary
Journal:  Childs Nerv Syst       Date:  2021-08-03       Impact factor: 1.475

  5 in total

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