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Tetraploidy in a 26-month-old girl (cytogenetic and molecular studies)

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2002
Authors
Guc-Scekić, M
Milašin, Jelena
Stevanović, M
Stojanov, LJ
Đorđević, M
Article (Published version)
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Abstract
Liveborn infants with tetraploidy are very rare in human pregnancies and usually die during the first days or months. Seven cases of liveborn infants with tetraploidy have previously been reported. Among them only two 92, XXXX infants survived for longer than 12 months. Here we report on the case of a 26-month-old girl with tetraploidy. The main clinical features of tetraploidy are facial dysmorphism, severely delayed growth and developmental delay. On the basis of molecular studies we discuss the possible origin of the additional chromosome sets in our proband. To our knowledge, this infant is the first reported case of tetraploidy who lived up to 26 months.
Keywords:
constitutive tetraploidy / humans
Source:
Clinical Genetics, 2002, 61, 1, 62-65
Publisher:
  • Wiley, Hoboken

DOI: 10.1034/j.1399-0004.2002.610112.x

ISSN: 0009-9163

PubMed: 11903358

WoS: 000174828700015

Scopus: 2-s2.0-0036461305
[ Google Scholar ]
27
20
URI
https://smile.stomf.bg.ac.rs/handle/123456789/1141
Collections
  • Radovi istraživača
Institution/Community
Stomatološki fakultet
TY  - JOUR
AU  - Guc-Scekić, M
AU  - Milašin, Jelena
AU  - Stevanović, M
AU  - Stojanov, LJ
AU  - Đorđević, M
PY  - 2002
UR  - https://smile.stomf.bg.ac.rs/handle/123456789/1141
AB  - Liveborn infants with tetraploidy are very rare in human pregnancies and usually die during the first days or months. Seven cases of liveborn infants with tetraploidy have previously been reported. Among them only two 92, XXXX infants survived for longer than 12 months. Here we report on the case of a 26-month-old girl with tetraploidy. The main clinical features of tetraploidy are facial dysmorphism, severely delayed growth and developmental delay. On the basis of molecular studies we discuss the possible origin of the additional chromosome sets in our proband. To our knowledge, this infant is the first reported case of tetraploidy who lived up to 26 months.
PB  - Wiley, Hoboken
T2  - Clinical Genetics
T1  - Tetraploidy in a 26-month-old girl (cytogenetic and molecular studies)
VL  - 61
IS  - 1
SP  - 62
EP  - 65
DO  - 10.1034/j.1399-0004.2002.610112.x
ER  - 
@article{
author = "Guc-Scekić, M and Milašin, Jelena and Stevanović, M and Stojanov, LJ and Đorđević, M",
year = "2002",
abstract = "Liveborn infants with tetraploidy are very rare in human pregnancies and usually die during the first days or months. Seven cases of liveborn infants with tetraploidy have previously been reported. Among them only two 92, XXXX infants survived for longer than 12 months. Here we report on the case of a 26-month-old girl with tetraploidy. The main clinical features of tetraploidy are facial dysmorphism, severely delayed growth and developmental delay. On the basis of molecular studies we discuss the possible origin of the additional chromosome sets in our proband. To our knowledge, this infant is the first reported case of tetraploidy who lived up to 26 months.",
publisher = "Wiley, Hoboken",
journal = "Clinical Genetics",
title = "Tetraploidy in a 26-month-old girl (cytogenetic and molecular studies)",
volume = "61",
number = "1",
pages = "62-65",
doi = "10.1034/j.1399-0004.2002.610112.x"
}
Guc-Scekić, M., Milašin, J., Stevanović, M., Stojanov, L.,& Đorđević, M.. (2002). Tetraploidy in a 26-month-old girl (cytogenetic and molecular studies). in Clinical Genetics
Wiley, Hoboken., 61(1), 62-65.
https://doi.org/10.1034/j.1399-0004.2002.610112.x
Guc-Scekić M, Milašin J, Stevanović M, Stojanov L, Đorđević M. Tetraploidy in a 26-month-old girl (cytogenetic and molecular studies). in Clinical Genetics. 2002;61(1):62-65.
doi:10.1034/j.1399-0004.2002.610112.x .
Guc-Scekić, M, Milašin, Jelena, Stevanović, M, Stojanov, LJ, Đorđević, M, "Tetraploidy in a 26-month-old girl (cytogenetic and molecular studies)" in Clinical Genetics, 61, no. 1 (2002):62-65,
https://doi.org/10.1034/j.1399-0004.2002.610112.x . .

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