Literature DB >> 15596773

Generalized dystonia and striatal calcifications with lipoid proteinosis.

H A G Teive1, E R Pereira, J A A Zavala, M C Lange, L de Paola, S Raskin, L C Werneck, T Hamada, J A McGrath.   

Abstract

Lipoid proteinosis (LP) is an autosomal recessive disease that typically presents with papular, verrucous, poxlike, or acneiform scars and lesions and hoarseness. LP was recently mapped to the 1q21 locus and shown to result from mutations in the extracellular matrix protein 1 gene (ECM1). Epilepsy, mental retardation, and hippocampal calcifications can occur. The authors describe a patient with generalized dystonia caused by striatal calcifications.

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Year:  2004        PMID: 15596773     DOI: 10.1212/01.wnl.0000145602.64073.c2

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  4 in total

1.  Assessment of dynamic thiol-disulfide homeostasis in patients with lipoid proteinosis (Urbach-Wiethe syndrome).

Authors:  Seyhan Taskin; Hakim Celik; Abdullah Taskin; Mustafa Aksoy; Isa An; Yavuz Yesilova
Journal:  Rev Assoc Med Bras (1992)       Date:  2022-09       Impact factor: 1.712

2.  Amygdalae and striatum calcification in lipoid proteinosis.

Authors:  F G Gonçalves; M B de Melo; V de L Matos; F R Barra; R E Figueroa
Journal:  AJNR Am J Neuroradiol       Date:  2009-08-20       Impact factor: 3.825

3.  Molecular analysis of lipoid proteinosis: identification of a novel nonsense mutation in the ECM1 gene in a Pakistani family.

Authors:  Muhammad Nasir; Amir Latif; Muhammad Ajmal; Reem Qamar; Muhammad Naeem; Abdul Hameed
Journal:  Diagn Pathol       Date:  2011-07-26       Impact factor: 2.644

4.  Lipoid Proteinosis (Urbach-Wiethe Disease): A Rare Genodermatosis with Characteristic Dermatological and Neuroimaging Findings.

Authors:  Aparajita Chatterjee; Lakshminarayanapuram G Viswanathan; Madhu Nagappa; Sanjib Sinha
Journal:  Ann Indian Acad Neurol       Date:  2021-03-24       Impact factor: 1.383

  4 in total

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