Results 161 to 170 of about 48,299 (209)
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Clinical Genetics, 1976
Clinical signs of a partial trisomy of the long arm of a chromosome 13 were present in a boy with a “de novo” translocation 13p+/13q‐.
C, Stoll +3 more
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Clinical signs of a partial trisomy of the long arm of a chromosome 13 were present in a boy with a “de novo” translocation 13p+/13q‐.
C, Stoll +3 more
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BJOG: An International Journal of Obstetrics & Gynaecology, 1992
ABSTRACTObjective To assess the reported association between field trisomy 13 and maternal pre‐eclampsia.Design A retrospective case‐control study.Subjects Twenty‐five women who gave birth to trisomy 13 infants in southwest England between 1971 and 1989; 38 women who gave birth to trisomy 18 infants in the same region over the same ...
J F, Tuohy, D K, James
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ABSTRACTObjective To assess the reported association between field trisomy 13 and maternal pre‐eclampsia.Design A retrospective case‐control study.Subjects Twenty‐five women who gave birth to trisomy 13 infants in southwest England between 1971 and 1989; 38 women who gave birth to trisomy 18 infants in the same region over the same ...
J F, Tuohy, D K, James
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European Journal of Obstetrics & Gynecology and Reproductive Biology, 1995
A 41 year old multiparous woman with an uncomplicated obstetric history was referred because of pre-eclampsia. As ultrasonic examination revealed severe IUGR and multiple congenital anomalies, trisomy 13 was suspected and confirmed by amniocentesis. This chromosomal anomaly should be suspected in cases where pre-eclampsia is associated with abnormal ...
R, Heydanus, P, Defoort, M, Dhont
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A 41 year old multiparous woman with an uncomplicated obstetric history was referred because of pre-eclampsia. As ultrasonic examination revealed severe IUGR and multiple congenital anomalies, trisomy 13 was suspected and confirmed by amniocentesis. This chromosomal anomaly should be suspected in cases where pre-eclampsia is associated with abnormal ...
R, Heydanus, P, Defoort, M, Dhont
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Leukemia & Lymphoma, 1992
Trisomy 13 occurring as a sole cytogenetic abnormality has recently been demonstrated to have adverse prognostic significance in acute leukemia. Trisomy 13 is seen primarily in an older male population, and has been reported in treatment-associated acute leukemia and acute leukemia evolved from myelodysplastic syndromes, as well as in de novo leukemia.
M R, Baer, C D, Bloomfield
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Trisomy 13 occurring as a sole cytogenetic abnormality has recently been demonstrated to have adverse prognostic significance in acute leukemia. Trisomy 13 is seen primarily in an older male population, and has been reported in treatment-associated acute leukemia and acute leukemia evolved from myelodysplastic syndromes, as well as in de novo leukemia.
M R, Baer, C D, Bloomfield
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Prenatal Diagnosis, 1986
AbstractPrune belly (urethral obstruction sequence) has previously been reported as an isolated malformation sequence, in association with trisomy 18 (Nevin et al., 1983) and more recently with trisomy 13 (Beckman et al., 1984). A further case associated with trisomy 13 in a fetus is reported.
C M, McKeown, D, Donnai
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AbstractPrune belly (urethral obstruction sequence) has previously been reported as an isolated malformation sequence, in association with trisomy 18 (Nevin et al., 1983) and more recently with trisomy 13 (Beckman et al., 1984). A further case associated with trisomy 13 in a fetus is reported.
C M, McKeown, D, Donnai
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2019
This chapter reviews the incidence, etiology, and chromosomal nature of Trisomy 13. Prenatal findings on US and the utility of cfcell free DNA for diagnosis and management of Trisomy 13 is discussed. The differential diagnosis for Trisomy 13 is not extensive and the diagnosis is usually possible on a clinical basis after assessment of the ...
Robin D. Clark, Cynthia J. Curry
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This chapter reviews the incidence, etiology, and chromosomal nature of Trisomy 13. Prenatal findings on US and the utility of cfcell free DNA for diagnosis and management of Trisomy 13 is discussed. The differential diagnosis for Trisomy 13 is not extensive and the diagnosis is usually possible on a clinical basis after assessment of the ...
Robin D. Clark, Cynthia J. Curry
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Clinical Pediatrics, 1969
A chromosomal abnormality should be suspected in every patient with multiple congenital anomalies. It is important to determine the specific type in order to provide the parents with a prognosis and proper genetic counseling. In patients with multiple congenital anomalies who have scalp defects, the most likely ...
D, Abuelo, M, Feingold
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A chromosomal abnormality should be suspected in every patient with multiple congenital anomalies. It is important to determine the specific type in order to provide the parents with a prognosis and proper genetic counseling. In patients with multiple congenital anomalies who have scalp defects, the most likely ...
D, Abuelo, M, Feingold
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2004
Die Trisomie 18 (Edwards-Syndrom, Erstbeschreibung 1960) ist nach dem Down-Syndrom die zweithaufigst vorkommende numerische Aneuploidie. Dabei ist das Chromosom 18 in jeder Korperzelle des Kindes dreifach vorhanden.
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Die Trisomie 18 (Edwards-Syndrom, Erstbeschreibung 1960) ist nach dem Down-Syndrom die zweithaufigst vorkommende numerische Aneuploidie. Dabei ist das Chromosom 18 in jeder Korperzelle des Kindes dreifach vorhanden.
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Trisomy 13: Changing Perspectives
Neonatal Network, 2016ABSTRACTThe diagnosis of trisomy 13 has been considered incompatible with life. Trisomy 13 is associated with a pattern of congenital anomalies and mental disabilities that make caring for these infants a challenge for both the family and health care professionals. The clinical management of trisomy 13 varies based on the organ systems involved.
Gabriel, Macias, Cheryl, Riley
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Berry Syndrome with Trisomy 13
Pediatric Cardiology, 2002We report on 2-day-old neonate with trisomy 13 with coexistent distal aortopulmonary septal defect, aortic origin of the right pulmonary artery, interrupted aortic arch, intact ventricular septum, and a patent ductus arteriosus diagnosed by two-dimensional and color Doppler echocardiography.
J, Sharma, M, Saleh, B B, Das
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