Literature DB >> 21808490

McLeod Syndrome: Report of an Indian family with phenotypic heterogeneity.

A Chakravarty1, P Bhattacharya, D Banerjee, S Mukherjee.   

Abstract

Entities:  

Year:  2011        PMID: 21808490      PMCID: PMC3141489          DOI: 10.4103/0972-2327.82827

Source DB:  PubMed          Journal:  Ann Indian Acad Neurol        ISSN: 0972-2327            Impact factor:   1.383


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Sir, We thank the authors[1] of the letter for their keen interest in our published report on McLeod Syndrome (MLS)[2]. It appears that the report mentioned by the authors of the letter had not been adequately cited in PUBMED. Moreover, a lack of molecular genetic data on the case would fall short of making a definitive diagnosis of MLS in the case mentioned. The family reported by us, therefore, appears to be the first genetically proved case of MLS reported from India.
  2 in total

1.  Mcleod syndrome: Report of an Indian family with phenotypic heterogeneity.

Authors:  Ambar Chakravarty; P Bhattacharya; D Banerjee; S Mukherjee
Journal:  Ann Indian Acad Neurol       Date:  2011-01       Impact factor: 1.383

2.  McLeod syndrome and acanthocytosis.

Authors:  M Mehndiratta
Journal:  Ann Indian Acad Neurol       Date:  2011-04       Impact factor: 1.383

  2 in total
  1 in total

1.  The first report of a Chinese family with McLeod syndrome.

Authors:  Bik Ling Man; Yuet Ping Yuen; Yat Pang Fu
Journal:  BMJ Case Rep       Date:  2014-06-03
  1 in total

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