Cavalanti Gomes

Learn More
Absence of band 3, associated with the mutation Coimbra (V488M) in the homozygous state, caused severe hereditary spherocytosis in a young child. Although prenatal testing was made available to the parents, it was declined. Because the fetus stopped moving near term, an emergency cesarean section was performed and a severely anemic, hydropic female baby was(More)
Four intragenic PKLR polymorphisms [1705A/C, 1738C/T. T10/19, and (ATT)n microsatellite] were studied in normal population samples of Central Portugal and São Tomé e Príncipe, a small archipelago located in the Gulf of Guinea, West Africa. For all loci, the observed genotype distributions do not deviate from Hardy-Weinberg equilibrium. The allele(More)
Objetivo: Estudo longitudinal, ultrassonográfico com modo B e Doppler, dos rins e fígado maternos na gravidez de baixo risco, para estabelecer, quantificar parâmetros de normalidade e correlacioná-los com as modificações fisiológicas. Materiais e Métodos: Foram examinadas 25 gestantes, realizando-se quatro exames em cada paciente no primeiro, segundo e(More)
  • 1