Chédiak-Higashi Syndrome: A Case Report
Chédiak-Higashi syndrome (CHS) is an extremely rare autosomal recessive immunodeficiency disorder. Approximately 200 cases have been reported worldwide. To the best of our knowledge, not more than 10 cases have been reported from India. Herein we are reporting a case of CHS in one-and-half-year-old...
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Veröffentlicht in: | Indian journal of hematology & blood transfusion 2013-06, Vol.29 (2), p.80-83 |
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creator | Patne, Shashikant C. U. Kumar, Sandip Bagri, Narendra Kumar Kumar, Ashok Shukla, Jyoti |
description | Chédiak-Higashi syndrome (CHS) is an extremely rare autosomal recessive immunodeficiency disorder. Approximately 200 cases have been reported worldwide. To the best of our knowledge, not more than 10 cases have been reported from India. Herein we are reporting a case of CHS in one-and-half-year-old boy who presented to us in the accelerated phase of disease. Other syndromes presenting with similar clinical features have also been discussed. |
doi_str_mv | 10.1007/s12288-011-0130-y |
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U.</creatorcontrib><creatorcontrib>Kumar, Sandip</creatorcontrib><creatorcontrib>Bagri, Narendra Kumar</creatorcontrib><creatorcontrib>Kumar, Ashok</creatorcontrib><creatorcontrib>Shukla, Jyoti</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>India Database</collection><collection>India Database: Health & Medicine</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Indian journal of hematology & blood transfusion</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Patne, Shashikant C. U.</au><au>Kumar, Sandip</au><au>Bagri, Narendra Kumar</au><au>Kumar, Ashok</au><au>Shukla, Jyoti</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chédiak-Higashi Syndrome: A Case Report</atitle><jtitle>Indian journal of hematology & blood transfusion</jtitle><stitle>Indian J Hematol Blood Transfus</stitle><addtitle>Indian J Hematol Blood Transfus</addtitle><date>2013-06</date><risdate>2013</risdate><volume>29</volume><issue>2</issue><spage>80</spage><epage>83</epage><pages>80-83</pages><issn>0971-4502</issn><issn>0974-0449</issn><eissn>0974-0449</eissn><eissn>0971-4502</eissn><abstract>Chédiak-Higashi syndrome (CHS) is an extremely rare autosomal recessive immunodeficiency disorder. Approximately 200 cases have been reported worldwide. To the best of our knowledge, not more than 10 cases have been reported from India. Herein we are reporting a case of CHS in one-and-half-year-old boy who presented to us in the accelerated phase of disease. 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source | SpringerNature Journals; EZB-FREE-00999 freely available EZB journals; PubMed Central |
subjects | Autoimmune diseases Blood Transfusion Medicine Case Report Hematology Human Genetics Medical diagnosis Medicine Medicine & Public Health Oncology Pediatrics |
title | Chédiak-Higashi Syndrome: A Case Report |
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