Double aneuploidy (48,XXY,+21) of maternal origin in a child born to a 13-year-old mother: evaluation of the maternal folate metabolism.
Biselli, J M
Double aneuploidy (48,XXY,+21) of maternal origin in a child born to a 13-year-old mother: evaluation of the maternal folate metabolism. [electronic resource] - Genetic counseling (Geneva, Switzerland) 2009 - 225-34 p. digital
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
1015-8146
Adolescent
Alleles
Aneuploidy
Brazil
Chromosomes, Human, X--genetics
Chromosomes, Human, Y--genetics
DNA Mutational Analysis
Down Syndrome--diagnosis
Female
Ferredoxin-NADP Reductase--genetics
Folic Acid--blood
Genetic Carrier Screening
Genotype
Heart Defects, Congenital--diagnosis
Homocysteine--blood
Homozygote
Humans
Infant
Klinefelter Syndrome--diagnosis
Male
Meiosis
Methylenetetrahydrofolate Reductase (NADPH2)--genetics
Methylmalonic Acid--blood
Nondisjunction, Genetic--genetics
Polymorphism, Genetic--genetics
Pregnancy
Pregnancy in Adolescence--genetics
Sex Chromosome Aberrations
Trisomy
Double aneuploidy (48,XXY,+21) of maternal origin in a child born to a 13-year-old mother: evaluation of the maternal folate metabolism. [electronic resource] - Genetic counseling (Geneva, Switzerland) 2009 - 225-34 p. digital
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
1015-8146
Adolescent
Alleles
Aneuploidy
Brazil
Chromosomes, Human, X--genetics
Chromosomes, Human, Y--genetics
DNA Mutational Analysis
Down Syndrome--diagnosis
Female
Ferredoxin-NADP Reductase--genetics
Folic Acid--blood
Genetic Carrier Screening
Genotype
Heart Defects, Congenital--diagnosis
Homocysteine--blood
Homozygote
Humans
Infant
Klinefelter Syndrome--diagnosis
Male
Meiosis
Methylenetetrahydrofolate Reductase (NADPH2)--genetics
Methylmalonic Acid--blood
Nondisjunction, Genetic--genetics
Polymorphism, Genetic--genetics
Pregnancy
Pregnancy in Adolescence--genetics
Sex Chromosome Aberrations
Trisomy