Literature DB >> 16080291

MRI and neurological findings in macrocephaly-cutis marmorata telangiectatica congenita syndrome: report of ten cases and review of the literature.

L Garavelli1, K Leask, C Zanacca, S Pedori, G Albertini, E Della Giustina, G F Croci, C Magnani, G Banchini, J Clayton-Smith, M Bocian, H Firth, J A Gold, J Hurst.   

Abstract

MRI and neurological findings in macrocephaly-cutis marmorata telangiectatica congenita syndrome: report of ten cases and review of the literature: We describe the clinical history and magnetic resonance imaging (MRI) findings in 10 children with the Macrocephaly-Cutis Marmorata Telangiectatica Congenita syndrome (M-CMTC--MIM 602501). This syndrome has recently been delineated within the general group of patients with Cutis Marmorata Telangiectatica (CMTC) as a distinct and easily recognisable entity. In contrast to most children with CMTC, patients with M-CMTC syndrome have a high risk of neurological abnormalities, such as hydrocephalus, megalencephaly, developmental delay and mental retardation. An MRI scan showed structural cerebral abnormalities in all of our patients, including megalencephaly, asymmetry of the cerebral hemispheres and abnormally increased signal of white matter. Seven patients also had Chiari type I malformation. Reviewing all reported cases, we propose appropriate surveillance for known complications.

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Mesh:

Year:  2005        PMID: 16080291

Source DB:  PubMed          Journal:  Genet Couns        ISSN: 1015-8146


  7 in total

Review 1.  Clinical review of genetic epileptic encephalopathies.

Authors:  Grace J Noh; Y Jane Tavyev Asher; John M Graham
Journal:  Eur J Med Genet       Date:  2012-01-25       Impact factor: 2.708

Review 2.  Tonsillar herniation spectrum: more than just Chiari I. Update and controversies on classification and management.

Authors:  Pietro Fiaschi; Giovanni Morana; Pasquale Anania; Andrea Rossi; Alessandro Consales; Gianluca Piatelli; Armando Cama; Marco Pavanello
Journal:  Neurosurg Rev       Date:  2019-11-10       Impact factor: 3.042

3.  Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome (MCAP): A Rare Dynamic Genetic Disorder.

Authors:  Kalyan Sarma; Manoj K Nayak; Biswamohan Mishra; Shailesh B Gaikwad
Journal:  Cureus       Date:  2022-05-18

4.  Hydrocephalus and Chiari type 1 malformation in macrocephaly-cutis marmorata telangiectatica congenita: a case-based update.

Authors:  Juan F Martínez-Lage; Encarna Guillén-Navarro; María-José Almagro; Matías Felipe-Murcia; Antonio López López-Guerrero; Marcelo Galarza
Journal:  Childs Nerv Syst       Date:  2009-09-10       Impact factor: 1.475

5.  Neuroimaging findings in macrocephaly-capillary malformation: a longitudinal study of 17 patients.

Authors:  Robert L Conway; Barry D Pressman; William B Dobyns; Moise Danielpour; John Lee; Pedro A Sanchez-Lara; Merlin G Butler; Elaine Zackai; Lindsey Campbell; Sulagna C Saitta; Carol L Clericuzio; Jeff M Milunsky; H Eugene Hoyme; Joseph Shieh; John B Moeschler; Barbara Crandall; Julie L Lauzon; David H Viskochil; Brian Harding; John M Graham
Journal:  Am J Med Genet A       Date:  2007-12-15       Impact factor: 2.802

6.  A combination of genetic and biochemical analyses for the diagnosis of PI3K-AKT-mTOR pathway-associated megalencephaly.

Authors:  Yutaka Negishi; Fuyuki Miya; Ayako Hattori; Yoshikazu Johmura; Motoo Nakagawa; Naoki Ando; Ikumi Hori; Takao Togawa; Kohei Aoyama; Kei Ohashi; Shinobu Fukumura; Seiji Mizuno; Ayako Umemura; Yoko Kishimoto; Nobuhiko Okamoto; Mitsuhiro Kato; Tatsuhiko Tsunoda; Mami Yamasaki; Yonehiro Kanemura; Kenjiro Kosaki; Makoto Nakanishi; Shinji Saitoh
Journal:  BMC Med Genet       Date:  2017-01-13       Impact factor: 2.103

7.  Megalencephaly-capillary malformation-polymicrogyria syndrome: the first case report in Korea.

Authors:  Yeon-Chul Choi; Mi-Sun Yum; Min-Jee Kim; Yun-Jung Lee; Tae-Sung Ko
Journal:  Korean J Pediatr       Date:  2016-11-30
  7 in total

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