Literature DB >> 24700663

The relative frequency of lysosomal storage disorders: a medical genetics referral laboratory's experience from India.

Srilatha Kadali1, Anusha Kolusu1, Maheshwar Reddy Gummadi1, Jayanthi Undamatla2.   

Abstract

Lysosomal storage disorders are a group of rare, genetically inherited metabolic disorders. Because the literature on epidemiologic data is scanty from India, we attempted to determine their relative frequency and regional distribution. Our retrospective study included 1558 patients with clinical suspicion of various lysosomal storage disorders referred to Sandor Lifesciences Pvt Ltd during 2007 to 2012. About 30% of the cases were tested positive, with sphingolipidoses as the most common subgroup, followed by mucopolysaccharidoses, and Gaucher disease as the most frequently occurring individual lysosomal storage disorder. Our data indicates that lysosomal storage disorders are more common in males than females and infants comprise the most common age group followed by juvenile. The burden of these disorders is predicted to be high in India because of the large population, coupled with the practice of consanguineous marriages. This study emphasizes the importance of epidemiologic studies in order to implement appropriate preventive measures.
© The Author(s) 2014.

Entities:  

Keywords:  inborn errors of metabolism; lysosomal storage disorders; mucopolysaccharidoses; prevalence; sphingolipidoses

Mesh:

Year:  2014        PMID: 24700663     DOI: 10.1177/0883073813515075

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


  7 in total

1.  Status of Newborn Screening and Inborn Errors of Metabolism in India.

Authors:  Seema Kapoor; B K Thelma
Journal:  Indian J Pediatr       Date:  2018-05-07       Impact factor: 1.967

2.  Spectrum of Lysosomal Storage Disorders at Tertiary Centre: Retrospective Case-Record Analysis.

Authors:  Ankur Singh; Rajniti Prasad; Om Prakash Mishra
Journal:  J Pediatr Genet       Date:  2020-01-02

3.  Lysosomal Storage Disorders in Egyptian Children.

Authors:  Mohamed A Elmonem; Iman G Mahmoud; Dina A Mehaney; Sahar A Sharaf; Sawsan A Hassan; Azza Orabi; Fadia Salem; Marian Y Girgis; Amira El-Badawy; Magy Abdelwahab; Zeinab Salah; Neveen A Soliman; Fayza A Hassan; Laila A Selim
Journal:  Indian J Pediatr       Date:  2016-02-02       Impact factor: 1.967

Review 4.  Genomics of rare genetic diseases-experiences from India.

Authors:  Sridhar Sivasubbu; Vinod Scaria
Journal:  Hum Genomics       Date:  2019-09-25       Impact factor: 4.639

5.  Twenty- five years of biochemical diagnosis of Gaucher disease: the Egyptian experience.

Authors:  Ekram Fateen; Zeinab Y Abdallah
Journal:  Heliyon       Date:  2019-11-01

6.  Lysosomal Storage Disorders: Clinical, Biochemical and molecular profile from Rare disease centre, India.

Authors:  Manisha Goyal; Ashok Gupta
Journal:  Ann Indian Acad Neurol       Date:  2021-03-27       Impact factor: 1.383

7.  Epidemiology of Sanfilippo syndrome: results of a systematic literature review.

Authors:  Tamás Zelei; Kata Csetneki; Zoltán Vokó; Csaba Siffel
Journal:  Orphanet J Rare Dis       Date:  2018-04-10       Impact factor: 4.123

  7 in total

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