Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters










Database
Language
Publication year range
1.
J Obstet Gynaecol Res ; 31(6): 540-6, 2005 Dec.
Article in English | MEDLINE | ID: mdl-16343256

ABSTRACT

AIM: Interactions between different determinants of alpha-thalassemia raises considerable problems, particularly during pregnancies where antenatal diagnosis is necessary. This study aims to determine the different types of deletional alpha-thalassemia and Hemoglobin Constant Spring (HbCS), and their frequency in Malays, Chinese and Indians in Malaysia. METHODS: DNA from 650 pregnant women from the Antenatal Clinic of the University of Malaya Medical Center in Kuala Lumpur, Malaysia who showed mean cell volume < or =89 fL and/or mean cell hemoglobin < or =28 pg were analyzed for the double alpha-globin gene South-East Asian deletion (--SEA), the -alpha3.7 and -alpha4.2 single alpha-globin gene deletions and HbCS. RESULTS: One hundred and three (15.8%) of the pregnant women were confirmed as alpha-thalassemia carriers: 25 (3.8%) were alpha-thalassemia-1 carriers with the --SEA/alphaalpha genotype, 64 (9.8%) were heterozygous for the -alpha3.7 rightward deletion (-alpha3.7/alphaalpha), four (0.6%) were heterozygous for the -alpha4.2 leftward deletion (-alpha4.2/alphaalpha), nine (1.4%) were heterozygous for HbCS (alphaCSalpha/alphaalpha) and one (0.2%) was compound heterozygous with the -alpha3.7/alphaCSalpha genotype. The double alpha-globin gene --SEA deletion was significantly higher in the Chinese (15%) compared to the Malays (2.5%) and not detected in the Indians studied. The -alpha3.7 deletion was distributed equally in the three races. HbCS and -alpha4.2 was observed only in the Malays. CONCLUSION: The data obtained gives a better understanding of the interactions of the different alpha-thalassemia determinants in the different ethnic groups, thus enabling more rapid and specific confirmation of alpha-thalassemia in affected pregnancies where antenatal diagnosis is necessary.


Subject(s)
Asian People/genetics , Pregnancy Complications, Hematologic/genetics , alpha-Thalassemia/complications , alpha-Thalassemia/genetics , Adolescent , Adult , Base Sequence , DNA/genetics , Female , Genetic Carrier Screening , Globins/genetics , Humans , Malaysia , Pregnancy , Pregnancy Complications, Hematologic/diagnosis , alpha-Thalassemia/diagnosis , alpha-Thalassemia/prevention & control
2.
J Obstet Gynaecol Res ; 28(4): 203-10, 2002 Aug.
Article in English | MEDLINE | ID: mdl-12452262

ABSTRACT

In this review, tuberculosis of the genital tract was diagnosed retrospectively in 11 females over 15 years. The presentations of nine cases are described. Seven of the nine cases presented with ascites, vague abdominal distension, weight loss and were misdiagnosed as ovarian carcinoma. Eight women had no relevant past history. A review on clinical presentations and diagnosis of pelvic tuberculosis is presented. We conclude that although the incidence of tuberculosis is uncommon in developed countries, its prevalence appears to be increasing worldwide. Therefore, clinicians should consider tuberculosis as a differential diagnosis when encountering clinical presentations of pelvic mass and ascites.


Subject(s)
Tuberculosis, Female Genital/diagnosis , Adult , Ascites/etiology , Diagnosis, Differential , Female , Humans , Medical Records , Middle Aged , Ovarian Neoplasms/diagnosis , Retrospective Studies , Tuberculosis, Female Genital/complications , Tuberculosis, Female Genital/pathology
SELECTION OF CITATIONS
SEARCH DETAIL
...