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Communication Ability in Persons with Trisomy 18 and Trisomy 13
AAC: Augmentative and Alternative Communication, 2012The purpose of this study was to assess communication abilities among a sample of 10 individuals with Trisomy 18 and Trisomy 13. These 10 individuals were diagnosed with Trisomy 18 (n = 8) or Trisomy 13 (n = 2) and had a mean age of 15.96 years. The sample consisted of one male and nine females. Caregivers completed a case history and reported on words
Jena Mcdaniel +2 more
exaly +3 more sources
American Journal of Medical Genetics Part A, 2007
AbstractTrisomy 13 is one of the most common trisomies in clinically recognized pregnancies and one of the few trisomies identified in liveborns, yet relatively little is known about the errors that lead to trisomy 13. Accordingly, we initiated studies to investigate the origin of the extra chromosome in 78 cases of trisomy 13.
Hall, Heather E. +9 more
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AbstractTrisomy 13 is one of the most common trisomies in clinically recognized pregnancies and one of the few trisomies identified in liveborns, yet relatively little is known about the errors that lead to trisomy 13. Accordingly, we initiated studies to investigate the origin of the extra chromosome in 78 cases of trisomy 13.
Hall, Heather E. +9 more
openaire +3 more sources
Teratology, 1982
AbstractThe fetal development of mice trisomic for chromosome 13 (Ts 13) was investigated. Trisomic fetuses were obtained from the progeny of male mice heterozygous for the two Robertsonian translocation chromosomes Rb (11.13)4Bnr and Rb (6.13)3Rma mated to “all acrocentric” NMRI females. Trisomic fetuses were found at all stages between days 12 and 19
Hongell, K, Gropp, A
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AbstractThe fetal development of mice trisomic for chromosome 13 (Ts 13) was investigated. Trisomic fetuses were obtained from the progeny of male mice heterozygous for the two Robertsonian translocation chromosomes Rb (11.13)4Bnr and Rb (6.13)3Rma mated to “all acrocentric” NMRI females. Trisomic fetuses were found at all stages between days 12 and 19
Hongell, K, Gropp, A
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Radiology, 1969
In April 1960, Patau and others described a characteristic pattern of numerous anomalies associated with a trisomy in the 13–15 group (also known as D1 trisomy) (13). Although there have been over thirty published examples of trisomy 13–15, only brief mention of the disorder has been made in the radiological literature (1).
A E, James +3 more
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In April 1960, Patau and others described a characteristic pattern of numerous anomalies associated with a trisomy in the 13–15 group (also known as D1 trisomy) (13). Although there have been over thirty published examples of trisomy 13–15, only brief mention of the disorder has been made in the radiological literature (1).
A E, James +3 more
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Teratology, 1990
AbstractA significant number of fetuses with trisomy 13 are spontaneously or voluntarily lost before birth; however, very few such fetuses have been systemically autopsied. In the present study, ten trisomy 13 fetuses of 130–305 mm in crown‐rump length, estimated gestational age from 108 days to 239 days, were examined following either karyotype or ...
M, Fujinaga +2 more
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AbstractA significant number of fetuses with trisomy 13 are spontaneously or voluntarily lost before birth; however, very few such fetuses have been systemically autopsied. In the present study, ten trisomy 13 fetuses of 130–305 mm in crown‐rump length, estimated gestational age from 108 days to 239 days, were examined following either karyotype or ...
M, Fujinaga +2 more
openaire +2 more sources
NeoReviews, 2012
In this paper, we review the complex medical, ethical, and psychosocial decisions that confront maternal fetal medicine specialists, neonatologists, parents, nurses, and other providers in the management of infants diagnosed with two chromosomal conditions generally considered as lethal anomalies.
T. Allen Merritt +5 more
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In this paper, we review the complex medical, ethical, and psychosocial decisions that confront maternal fetal medicine specialists, neonatologists, parents, nurses, and other providers in the management of infants diagnosed with two chromosomal conditions generally considered as lethal anomalies.
T. Allen Merritt +5 more
openaire +1 more source
Trisomy 13/trisomy 18 mosaicism in an infant
Clinical Genetics, 1996Cytogenetic analysis of amniotic fluid cells from a 31‐week‐old fetus suffering from polyhydramnios revealed that there were two cell lines, each with either trisomy 13 or trisomy 18. We studied the origin and mechanism of formation of this unique mixoploidy by tracing chromosomal heteromorphisms as genetic markers, and showed no discordance of parent ...
K, Abe +4 more
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Recurrences of trisomy 18 and trisomy 13 after trisomy 21
Human Genetics, 1989Between 40 years and 43 years of age, a woman had three consecutive pregnancies with different prenatally diagnosed autosomal trisomies. This is compatible with the view that the predisposition to non-disjunction is not chromosome-specific.
D R, FitzPatrick, E, Boyd
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Trisomy 13 and myelodysplastic syndrome
Cancer Genetics and Cytogenetics, 1990The clinical and cytogenetic data of a patient with myelodysplastic syndrome-refractory anemia with excess blasts (MDS-RAEB) and trisomy 13 as the sole abnormality are presented. This appears to be only the second report of such a patient. The presence of trisomy 13 is confirmed by in situ hybridization using an alphoid repeat probe L1.26, which is ...
G C, Beverstock +4 more
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