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LETTER TO THE EDITOR |
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Year : 2011 | Volume
: 14
| Issue : 2 | Page : 144 |
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McLeod Syndrome: Report of an Indian family with phenotypic heterogeneity
A Chakravarty1, P Bhattacharya2, D Banerjee1, S Mukherjee2
1 Department of Neurology and Hematology, Vivekananda Institute of Medical Sciences, Kolkata, India 2 Department of Transfusion Medicine and Hematology, AMRI Hospitals, Kolkata, India
Date of Web Publication | 7-Jul-2011 |
Correspondence Address: A Chakravarty 1E 1202 AVISHIKTAII, Kolkata - 700 078 India
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/0972-2327.82827
How to cite this article: Chakravarty A, Bhattacharya P, Banerjee D, Mukherjee S. McLeod Syndrome: Report of an Indian family with phenotypic heterogeneity. Ann Indian Acad Neurol 2011;14:144 |
How to cite this URL: Chakravarty A, Bhattacharya P, Banerjee D, Mukherjee S. McLeod Syndrome: Report of an Indian family with phenotypic heterogeneity. Ann Indian Acad Neurol [serial online] 2011 [cited 2021 Feb 26];14:144. Available from: https://www.annalsofian.org/text.asp?2011/14/2/144/82827 |
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.
References | |  |
1. | Mehndiratta M. McLeod syndrome and Acanthocytosis. Ann Indian Acad Neurol 2011;14:143.  |
2. | Chakravarty A, Bhattacharya P, Banerjee D, Mukherjee S. McLeod Syndrome: Report of an Indian Family with Phenotypic Heterogeneity. Ann Indian Acad Neurol 2011;14:53-5.  [PUBMED] |
This article has been cited by | 1 |
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| Authors of Document Adurthi, S., Mahadevan, A., Bantwal, R., (...), Nath, A., Jayshree, R.S. | | Annals of Indian Academy of Neurology. 211; | | [Pubmed] | |
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