Double trisomy (48,XXX, 18)

48,XXX, +18 double trisomy – PubMed Central (PMC)

48,XXX, +18 double trisomy D. P. Madahar , Harvey Dosik , and Irving Wexler The Department of Pediatrics and The Division of Hematology, The Jewish Hospital and Medical Center of Brooklyn, and the Department of Pediatrics and Medicine, State University of …

Double trisomy 48,XXX,+18 in a newborn – Rosenfeld – 1981

We report the 6th case of double trisomy X and 18, ie, 48,XXX,+18. The infant lacked overlapping fingers, simian creases, and structural heart disease and …

An infant with double trisomy (48,XXX,+18) (Journal

We report an infant with double trisomy 48,XXX,+18, who also displayed features of Roberts syndrome. All previously published cases with similar double trisomy have presented with features of trisomy 18 syndrome. The chromosome analysis done at birth revealed the double trisomy…

Double trisomy 48,XXX,+ 18 in a newborn.

Double trisomy 48,XXX,+ 18 in a newborn. Rosenfeld W, Verma RS, Jhaveri RC, Salazar D, Dosik H. We report the 6th case of double trisomy X and 18 ie, 48,XXX,+ 18. The infant lacked overlapping fingers, simian creases, and structural heart disease and …

Double trisomy 48,XXX,+18 with multiple dysmorphic

Conclusion. These data suggested that in patients with clinical features similar to trisomy 18, especially with anomalies of the ears and/or reproductive malformations, double trisomy (48,XXX,+18) should be considered and karyotyping should be performed although it is a rare disease.

Double trisomy 48,XXX,+18 in a newborn | Request PDF

We report the 6th case of double trisomy X and 18 ie, 48,XXX,+ 18. The infant lacked overlapping fingers, simian creases, and structural heart disease and is alive at 275 days.

48,XXX, +18 double trisomy – researchgate.net

Chromosomal abnormality is a common cause of congenital anomalies, psychiatric disorders, and mental retardation. However, the double trisomy 48,XXX,+18 is a rare chromosome abnormality.

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Double trisomy 48,XXX,+18 with multiple dysmorphic features

with the double trisomy 48,XXX,+18. The literature on 16 fetuses or infants with the 48,XXX,+18 were also reviewed. Conclusion: These data suggested that in patients with clinical features similar to trisomy 18, especially with anomalies of the ears and/or reproductive malformations, double trisomy (48,XXX,+18) should be considered and

Published in: World Journal of Pediatrics · 2015Authors: Ziyan Jiang · Xiaohui Wu · Chaochun ZouAffiliation: Zhejiang UniversityAbout: Chromosome abnormality

Placental Histomorphology in a Case of Double Trisomy 48

Consequently, double trisomy X/18 is significantly less common, and, as a result, only a handful of cases of double trisomy 48,XXX,+18 have been reported in the literature. The rate of all double trisomies in karyotyped spontaneous abortions is reported to range from 0.21% to 2.8% [ 10 ].

Double trisomy 48,XXX,+18 in association with increased

Victor Dezerega, Cecilia Be, Amy E. Wong, Rafael Silva and Waldo Sepulveda, Prenatal Diagnosis of Double Trisomy 48,XXX,+18 in the First Trimester, Journal of …

Double trisomy 48,XXX,+18 in a newborn – DeepDyve

10.1002/ajmg.1320080109.abs We report the 6th case of double trisomy X and 18, ie, 48,XXX,+18. The infant lacked overlapping fingers, simian creases, and structural heart disease and is alive at 275 days. Two X chromosomes were late replicating.

Published in: American Journal of Medical Genetics · 1981Authors: Warren Rosenfeld · Warren Rosenfeld · Ram S Verma · Ramesh C Jhaveri · Delfor Sa…Affiliation: State University of New York System · Jewish Hospital