Literature DB >> 10728208

Merosin-positive congenital muscular dystrophy with mental retardation and cataracts: a new entity in two families.

H Topaloğlu1, M Yetük, B Talim, Z Akçören, M Cağlar.   

Abstract

Merosin-positive congenital muscular dystrophy is a heterogenous group of disorders with varying clinical presentations and severity. In general, central nervous system involvement is not present. There is also evidence for still unclassified forms. Here we report three cases in two families with merosin-positive congenital muscular dystrophy, mild mental retardation, bilateral cataracts and normal cranial magnetic resonance imaging. To our knowledge, such an association has not been reported previously, and thus is a new entity within congenital muscular dystrophy nosology.

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Year:  1997        PMID: 10728208     DOI: 10.1016/s1090-3798(97)80045-1

Source DB:  PubMed          Journal:  Eur J Paediatr Neurol        ISSN: 1090-3798            Impact factor:   3.140


  3 in total

1.  Biochemical and biomechanical characteristics of dystrophin-deficient mdx3cv mouse lens.

Authors:  Shruthi Karnam; Nikolai P Skiba; Ponugoti V Rao
Journal:  Biochim Biophys Acta Mol Basis Dis       Date:  2020-10-27       Impact factor: 5.187

2.  Mutations in INPP5K, Encoding a Phosphoinositide 5-Phosphatase, Cause Congenital Muscular Dystrophy with Cataracts and Mild Cognitive Impairment.

Authors:  Manuela Wiessner; Andreas Roos; Christopher J Munn; Ranjith Viswanathan; Tamieka Whyte; Dan Cox; Benedikt Schoser; Caroline Sewry; Helen Roper; Rahul Phadke; Chiara Marini Bettolo; Rita Barresi; Richard Charlton; Carsten G Bönnemann; Osório Abath Neto; Umbertina C Reed; Edmar Zanoteli; Cristiane Araújo Martins Moreno; Birgit Ertl-Wagner; Rolf Stucka; Christian De Goede; Tamiris Borges da Silva; Denisa Hathazi; Margherita Dell'Aica; René P Zahedi; Simone Thiele; Juliane Müller; Helen Kingston; Susanna Müller; Elizabeth Curtis; Maggie C Walter; Tim M Strom; Volker Straub; Kate Bushby; Francesco Muntoni; Laura E Swan; Hanns Lochmüller; Jan Senderek
Journal:  Am J Hum Genet       Date:  2017-02-09       Impact factor: 11.025

3.  Mutations in INPP5K Cause a Form of Congenital Muscular Dystrophy Overlapping Marinesco-Sjögren Syndrome and Dystroglycanopathy.

Authors:  Daniel P S Osborn; Heather L Pond; Neda Mazaheri; Jeremy Dejardin; Christopher J Munn; Khaloob Mushref; Edmund S Cauley; Isabella Moroni; Maria Barbara Pasanisi; Elizabeth A Sellars; R Sean Hill; Jennifer N Partlow; Rebecca K Willaert; Jaipreet Bharj; Reza Azizi Malamiri; Hamid Galehdari; Gholamreza Shariati; Reza Maroofian; Marina Mora; Laura E Swan; Thomas Voit; Francesco J Conti; Yalda Jamshidi; M Chiara Manzini
Journal:  Am J Hum Genet       Date:  2017-02-09       Impact factor: 11.025

  3 in total

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