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1.
J Assist Reprod Genet ; 34(4): 517-524, 2017 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-28108842

RESUMEN

PURPOSE: The aim of this study was to evaluate a new predisposition factor, M2/ANXA5 (RPRGL3), in recurrent pregnancy loss (RPL) patients of Malay origin, since it was previously known that the prevalence of this condition is relatively high among the Malay population of Malaysia, where conventional hereditary thrombophilia factors have been generally ruled out. METHODS: A total of 232 women who had experienced ≥2 unexplained RPL and 141 available male partners were recruited, with 360 healthy Malay and 166 parous female controls. Prevalence of M2 carriage and RPL odds ratios were calculated in (a) control and patient groups; (b) clinically defined subgroups in categories of pregnancy loss, primary, secondary, and tertiary; and (c) timing of pregnancy loss in early, ≤15th gestation week and "late" fetal losses, and >15th gestation week subgroups. RESULTS: Both male and female subjects had similar M2/ANXA5 allele frequencies. The carrier rate of M2/ANXA5 for the general Malay population was 42.2 and 34.9% for parous controls. These carrier rates compared to Malay RPL subjects (52% M2 carriers) resulted in elevated odds ratios (95% confidence interval) of 1.53 (1.1 to 2.1) and 1.97 (1.3 to 3.1) accordingly for early fetal losses. Moreover, exceeding copy numbers of M2/ANXA5 alleles seemed to afflict a greater chance of RPL in couples, especially when both partners were M2 carriers. CONCLUSION: This study confirmed the proposed role of M2/ANXA5 as embryonic, genetically associated thrombophilia predisposition factor for early RPL among ethnic Malay of Malaysia.


Asunto(s)
Aborto Habitual/genética , Anexina A5/genética , Predisposición Genética a la Enfermedad , Pruebas Genéticas , Aborto Habitual/fisiopatología , Adulto , Femenino , Frecuencia de los Genes/genética , Genotipo , Haplotipos , Heterocigoto , Humanos , Masculino , Embarazo , Factores de Riesgo , Adulto Joven
3.
Med J Malaysia ; 66(5): 510-2, 2011 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-22390115

RESUMEN

An acardiac twin is rare and the diagnosis is commonly achieved from antenatal ultrasound (US) scans. However there have been cases where the appearances of the acardiac twin can be confusing and mimics a mass or tumour, for example, a teratoma. We experienced a case where the findings were unclear from the antenatal ultrasound scans and we had to resort to Magnetic Resonance Imaging (MRI), where we finally made the correct diagnosis based on the identification of two umbilical cords, supplying the normal fetus and the 'mass' (acardiac twin) respectively.


Asunto(s)
Cardiopatías Congénitas/diagnóstico , Imagen por Resonancia Magnética , Ultrasonografía Prenatal , Adulto , Diagnóstico Diferencial , Femenino , Cardiopatías Congénitas/diagnóstico por imagen , Humanos , Embarazo , Embarazo Múltiple
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