Literature DB >> 12509711

Lysosomal storage disorders: diagnostic dilemmas and prospects for therapy.

David A Wenger1, Stephanie Coppola, Shu-Ling Liu.   

Abstract

PURPOSE: The main purpose of this review is to address some concerns regarding the accurate and timely diagnosis of lysosomal storage disorders (LSD).
METHODS: Using their experience in diagnosing LSD in more than 2500 individuals, the authors highlight several diagnostic difficulties and solutions and review the latest methods for early diagnosis and treatment.
RESULTS: While "classic" patients can be accurately diagnosed using relatively simple methods in an experienced laboratory, atypical patients require more detailed studies. With a few exceptions, almost all LSD can be diagnosed in leukocytes or plasma. Methods for screening all newborns without a family history of a LSD have been proposed, but such screening may require a large amount of effort for little gain.
CONCLUSIONS: With effective therapy becoming available for some LSD, early diagnosis is critically important. If the goal is to prevent serious complications related to the nervous and skeletal systems, earlier diagnosis is potentially advantageous. Accurate prognosis and assessing the need for aggressive therapy in newly diagnosed patients are problems that need further study.

Entities:  

Mesh:

Year:  2002        PMID: 12509711     DOI: 10.1097/00125817-200211000-00003

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  9 in total

1.  Lysosomal storage diseases: heterogeneous group of disorders.

Authors:  David A Wenger; Paola Luzi; Mohammad A Rafi
Journal:  Bioimpacts       Date:  2013-12-02

Review 2.  Chaperone-mediated autophagy in health and disease.

Authors:  Maria Kon; Ana Maria Cuervo
Journal:  FEBS Lett       Date:  2009-12-22       Impact factor: 4.124

3.  Preimplantation diagnosis of a lysosomal storage disorder by in situ enzymatic activity: 'proof of principle' in acid sphingomyelinase-deficient mice.

Authors:  A Butler; S C Henderson; R E Gordon; A Dagan; S Gatt; E H Schuchman
Journal:  J Inherit Metab Dis       Date:  2005       Impact factor: 4.982

4.  Selective screening for lysosomal storage diseases with dried blood spots collected on filter paper in 4,700 high-risk colombian subjects.

Authors:  Alfredo Uribe; Roberto Giugliani
Journal:  JIMD Rep       Date:  2013-04-23

Review 5.  Chaperone-mediated autophagy: selectivity pays off.

Authors:  Ana Maria Cuervo
Journal:  Trends Endocrinol Metab       Date:  2009-10-24       Impact factor: 12.015

6.  Enzymatic Screening and Diagnosis of Lysosomal Storage Diseases.

Authors:  Chunli Yu; Qin Sun; Hui Zhou
Journal:  N Am J Med Sci (Boston)       Date:  2013

7.  Enzyme replacement therapy in India: Lessons and insights.

Authors:  M Muranjan; S Karande
Journal:  J Postgrad Med       Date:  2018 Oct-Dec       Impact factor: 1.476

Review 8.  Biology of adeno-associated viral vectors in the central nervous system.

Authors:  Giridhar Murlidharan; Richard J Samulski; Aravind Asokan
Journal:  Front Mol Neurosci       Date:  2014-09-19       Impact factor: 5.639

9.  Report of a Case that Expands the Phenotype of Infantile Krabbe Disease.

Authors:  Marwan Nashabat; Sultan Al-Khenaizan; Majid Alfadhel
Journal:  Am J Case Rep       Date:  2019-05-04
  9 in total

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