Literature DB >> 17690079

Merosin-negative congenital muscular dystrophy: diffusion-weighted imaging findings of brain.

Alpay Alkan1, Ahmet Sigirci, Ramazan Kutlu, Mehmet Aslan, Selim Doganay, Cengiz Yakinci.   

Abstract

Merosin-negative congenital muscular dystrophy is a rare genetic disease of childhood involving the central and peripheral nervous system. There were high signal intensities throughout the centrum semiovale, periventricular, and sub-cortical white matters on T2-weighted images in a 4-year-old girl with merosin-negative congenital muscular dystrophy. An apparent diffusion coefficient map revealed increased signal intensity and apparent diffusion coefficient values in the periventricular and deep white matters. It may be attributable to increased water content in the white matter because of an abnormal blood-brain barrier rather than to decreased or abnormal myelination.

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Year:  2007        PMID: 17690079     DOI: 10.1177/0883073807303219

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


  5 in total

1.  Child with Isolated Motor Delay: Look at the Neuroimage.

Authors:  Indar Kumar Sharawat; Ananthanarayanan Kasinathan; Naveen Sankhyan
Journal:  Indian J Pediatr       Date:  2018-05-22       Impact factor: 1.967

Review 2.  Establishment and Dysfunction of the Blood-Brain Barrier.

Authors:  Zhen Zhao; Amy R Nelson; Christer Betsholtz; Berislav V Zlokovic
Journal:  Cell       Date:  2015-11-19       Impact factor: 41.582

Review 3.  Laminin-deficient muscular dystrophy: Molecular pathogenesis and structural repair strategies.

Authors:  Peter D Yurchenco; Karen K McKee; Judith R Reinhard; Markus A Rüegg
Journal:  Matrix Biol       Date:  2017-11-27       Impact factor: 11.583

4.  Cobblestone Malformation in LAMA2 Congenital Muscular Dystrophy (MDC1A).

Authors:  Himali Jayakody; Sanam Zarei; Huy Nguyen; Joline Dalton; Kelly Chen; Louanne Hudgins; John Day; Kara Withrow; Arti Pandya; Jean Teasley; William B Dobyns; Katherine D Mathews; Steven A Moore
Journal:  J Neuropathol Exp Neurol       Date:  2020-09-01       Impact factor: 3.685

Review 5.  Towards Central Nervous System Involvement in Adults with Hereditary Myopathies.

Authors:  Jens Reimann; Cornelia Kornblum
Journal:  J Neuromuscul Dis       Date:  2020
  5 in total

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