Israel the chosen few: A case of 42-year-old male with Hemoglobin H Disease / (Record no. 13208)

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000 -LEADER
fixed length control field 02200nam a22002537a 4500
001 - CONTROL NUMBER
control field R000781
003 - CONTROL NUMBER IDENTIFIER
control field PILC
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20241111093640.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 241111b |||||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Language of cataloging eng
Transcribing agency FEU-NRMF MEDICAL LIBRARY
Description conventions rda
050 ## - LIBRARY OF CONGRESS CALL NUMBER
Classification number MED 2024 0007
245 ## - TITLE STATEMENT
Title Israel the chosen few: A case of 42-year-old male with Hemoglobin H Disease /
Remainder of title [author] Diaren Marinela G. Bondoc
260 ## - PUBLICATION, DISTRIBUTION, ETC. (IMPRINT)
Place of publication, distribution, etc. Fairview, Quezon City;
Name of publisher, distributor, etc. Department of Internal Medicine, FEU-NRMF,
Date of publication, distribution, etc. 2024
300 ## - PHYSICAL DESCRIPTION
Dimensions in folder
Accompanying material with flash drive (soft copy)
336 ## - CONTENT TYPE
Source rdacontent
Content type term text
337 ## - MEDIA TYPE
Source rdamedia
Media type term unmediated
338 ## - CARRIER TYPE
Source rdacarrier
Carrier type term volume
504 ## - BIBLIOGRAPHY, ETC. NOTE
Bibliography, etc Includes bibliographical references
520 ## - SUMMARY, ETC.
Summary, etc. ABSTRACT<br/>Thalassemias are group of hemoglobinopathies caused by diminished or absent production of globin chains due to a genetic variant in one or more alpha or beta globin genes. There is ineffective erythropoiesis with intramedullary hemolysis due to this imbalance production of globin chain. Magnitude and severity of anemia and iron overload is due to the ineffective erythropoiesis (1). Increased hemolysis and mild to severe anemia with marked microcytosis and hypochromia are characteristic of Hemoglobin H disease. It is an intermediate form of alpha thalassemia and belongs to the group of non-transfusion-dependent thalassemia (2) Here we report a case of 42 year old male who initially presented with epigastric pain associated with symptoms of shortness of breath upon exertion, easy fatigability. Decreased Mean Concentration Volume (MCV), Mean Corpuscular Hemoglobin (MCH), Mean Corpuscular Hemoglobin Concentration (MCHC) and increase in Red Cell Distribution Width (RDW) can be seen in Complete Blood Complete (CBC). Early diagnosis of these cases are important to emphasize to patients to facilitate implementation of health care measures for prevention and immediate treatment of potentially serious hemolytic crisis.<br/>
521 ## - TARGET AUDIENCE NOTE
Target audience note Research - Department of Medicine
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Diaren Marinela G. Bondoc
Relator term author
856 ## - ELECTRONIC LOCATION AND ACCESS
Enable Ebook Yes
Text to speech No
Electronic format type pdf
Uniform Resource Identifier <a href="https://library.feu-nrmf.ph/cgi-bin/koha/opac-retrieve-file.pl?id=babd7b2592674c4848f55c72bef62de7">https://library.feu-nrmf.ph/cgi-bin/koha/opac-retrieve-file.pl?id=babd7b2592674c4848f55c72bef62de7</a>
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942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme Library of Congress Classification
Koha item type Research
Holdings
Withdrawn status Lost status Source of classification or shelving scheme Damaged status Not for loan Home library Current library Date acquired Total Checkouts Full call number Barcode Date last seen Price effective from Koha item type
    Library of Congress Classification     Far Eastern University - Nicanor Reyes Medical Foundation Far Eastern University - Nicanor Reyes Medical Foundation 11/11/2024   MED 2024 0007 R000781 11/11/2024 11/11/2024 Research