نتایج جستجو برای: thalassemia minor

تعداد نتایج: 102111  

Journal: :Scripta Scientifica Medica 2019

2017
Noor Mohammad Noori Iraj Shahramian Alireza Teimouri Mahmood Haghighat Seyed Mohsen Dehghani Elham Sharafi

Minor beta thalassemia is a common condition in children. The aim of the present study was the investigation of serum tissue transglutaminase IgA level as potential celiac disease in patients with thalassemia minor. This case control study was conducted on patients with beta thalassemia minor and healthy children in the years of 2014 to 2015. A total of 300 children were enrolled and IgA and ti...

2011
Monica Dogaru Daniel Coriu Trefor Higgins

The role of the laboratory in the diagnosis of thalassemia and hemoglobinopathies is crucial. The objective of our study was to compare two common methods used in hemoglobinopathy and thalassemia investigation. Hemoglobin electrophoresis and HPLC (high performance liquid chromatography) were used to investigate patients suspected with thalassemia. A total of 301 adult and child blood samples we...

Journal: :Iranian Journal of Blood and Cancer 2022

Thalassemia minor (MT), either β or α, is the most frequent single gene mutation in human beings affecting 6% of population worldwide. It more Mediterranean region, Africa and South-East Asia. On other hand Iron deficiency anemia (IDA), nutritional secondary to gastrointestinal menstrual bleeding, cause acquired anemia. Differentiation between these two types important because both them present...

Journal: :Annals of clinical and laboratory science 1983
W L Marsh Z R Rogers D P Nelson T S Vedvick

Recent immigrants from Southeast Asia were screened for hematologic abnormalities using a multichannel cell counter (Coulter S), peripheral smear, free erythrocyte protoporphyrin (FEP), isoelectric focusing, and a qualitative screen for glucose-6-phosphate dehydrogenase deficiency. Hematologic abnormalities were further defined by hemoglobin electrophoresis, globin electrophoresis, HbA2 levels,...

Journal: :Archives of Iranian medicine 2014
Fariba Ghahramani Yousef Alimohamadi Mohammad Mahboubi Abdolreza Afrasiabi

BACKGROUND Chorionic Villous Sampling (CVS) is a diagnostic method for determining genetic disorders. The present study aimed to determine the negative predictive value of the CVS in the diagnosis of major thalassemia in genetic laboratory of Dastgheib Hospital, Shiraz, Iran. METHODS The present research was an evaluation diagnostic test conducted on 372 records of embryos examined through CV...

Journal: :Bangladesh Medical Research Council bulletin 2010
Hassan Solhi Mojgan Hashemieh Mohammad Lorgard Dezfuli Nejad Hamid-Reza Khoddami Vishteh Maryam Rahmati Nejad

Rapid diagnosis of major beta thalassemia along with certain preventive measures is of utmost significance. The present study aims to compare the fingerprints in Major beta thalassemic patients (67) and in their parents (76 with minor thalassemia) with the normal fingerprints of control group (144). A forensic medical examiner determined fingerprint types of arch, loop, whorl and other types. L...

2013
H Hashemizadeh R Noori

BACKGROUND Beta thalassemia is a preventable disease. Iran has about 20,000Patients who are homozygote for β-thalassaemia and 3,750,000 carriers. The aim of this study was to determine the prevalence of beta thalassemia minor among men who underwent premarital screening in Quchana city in Khorasan Razavi region of Iran. MATERIALS AND METHODS This research is a descriptive cross-sectional stud...

2013
Che Ry Hong Hyoung Jin Kang Ji Won Lee Hyery Kim Nam Hee Kim Kyung Duk Park June Dong Park Moon-Woo Seong Sung Sup Park Hee Young Shin Hyo Seop Ahn

Few literatures have elaborated on the clinical characteristics of children with thalassemia from low-prevalence areas. A retrospective analysis was conducted on children genetically confirmed with thalassemia at Seoul National University Children's Hospital in Korea. Nine children (1α thalassemia trait, 6β thalassemia minor, 2β thalassemia intermedia) were diagnosed with thalassemia at median ...

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