EUROPEAN JOURNAL OF
PHARMACEUTICAL AND MEDICAL RESEARCH

( An ISO 9001:2015 Certified International Journal )

An International Peer Reviewed Journal for Pharmaceutical, Medical & Biological Sciences

An Official Publication of Society for Advance Healthcare Research (Reg. No. : 01/01/01/31674/16)

European Journal of Pharmaceutical and Medical Research (EJPMR) has indexed with various reputed international bodies like : Google Scholar , Indian Science Publications , InfoBase Index (In Process) , SOCOLAR, China , Research Bible, Fuchu, Tokyo. JAPAN , International Society for Research activity (ISRA) , Scientific Indexing Services (SIS) , Polish Scholarly Bibliography , Global Impact Factor (GIF) (Under Process) , Universal Impact Factor , International Scientific Indexing (ISI), UAE , Index Copernicus , CAS (A Division of American Chemical Society) USA (Under Process) , Directory of Open Access Journal (DOAJ, Sweden, in process) , UDLedge Science Citation Index , CiteFactor , Directory Of Research Journal Indexing (DRJI) , Indian citation Index (ICI) , Journal Index (JI, Under Process) , Directory of abstract indexing for Journals (DAIJ) , Open Access Journals (Under Process) , Impact Factor Services For International Journals (IFSIJ) , Cosmos Impact Factor , Jour Informatics (Under Process) , Eurasian Scientific Journal Index (ESJI) , International Innovative Journal Impact Factor (IIJIF) , Science Library Index, Dubai, United Arab Emirates , Pubmed Database [NLM ID: 101669306] (Under Process) , IP Indexing (IP Value 2.40) , Web of Science Group (Under Process) , Directory of Research Journals Indexing , Scholar Article Journal Index (SAJI) , International Scientific Indexing ( ISI ) , Scope Database , Academia ,

ISSN 2394-3211

Impact Factor: 7.065

ICV - 79.57

Abstract

UNEXPLAINED BLEEDING - MANIFESTATION OF GLANZMANN’S THROMBOSTHENIA

Dr. Priti Kamble*, Dr. Nivedita Patil , Dr. Yamini S., Dr Hashiq N. and Dr. Jaiprakash Jaiswa

ABSTRACT

Glanzmann’s thrombosthenia(GT) is a rare inherited platelet disorder characterized by deficiency of platelet fibrinogen receptor alpha IIb β3.[1] Here we report two cases of GT from single family born to parents with 3 degree consanguineous marriage. Among the two cases, older sibling i.e 3.5years old female child presented with ecchymosis and epistaxis and second patient, her younger brother aged 1 year had history of gum bleeding and ecchymosis. GT is rare bleeding disorder. Still, in a case of unexplained bleeding in a child, one should suspect platelet function disorder. With proper supportive care Glanzmann’s thrombasthenia has a very good prognosis.[2]

Keywords: .

[Full Text Article] [Download Certificate]