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A dysmorphic newborn with 45,X,der(1)inv(1)(p13;qter)t(Y;1)(pter -> 4q11;p13),-Y De novo karyotype
- Publication Year :
- 2005
- Publisher :
- Medecine et Hygiene, 2005.
-
Abstract
- A dysmorphic newborn with 45,x,der(1)inv,(1)(p13;qter)t(y;1)(pter -> q11;p13),-Y de novo karyotype: Y/autosome translocations are very rare chromosomal rearrangements. In most cases, the long arm of the Y chromosome is translocated onto an autosome and most patients are referred because of male infertility. Y/1 translocations are very rare, and have been reported in seven patients sofar. Pericentric inversions may be seen In all chromosomes and are not associated with phenotypic abnormalities. Here we report a 6-day old male baby with prenatal growth retardation, frontal bossing, hypertelorism. micrognathia, cleft soft palate, absent uvula, hypospadias, simian line in both hands and hammer toes. Cytogenetic analysis was performed with GTG-banding, C-banding and FISH analysis containing X centromeric probe, Yq12-qter locus specific probe and whole chromosome Y probe. An unbalanced Y/1 translocation was diagnosed: 45,X,der(1)inv(1)(p13:qter)t(y;1)(pter -> q11:p13),-Y.
- Subjects :
- Male
Chromosome banding
Pericentric chromosome inversion
Unbalanced Y/1 translocation
Medical ethics
Gene locus
Infant, newborn
Chromosome translocation
Abnormalities, multiple
DNA mutational analysis
Y/autosome translocation
Seminal plasma proteins
Male Sterility Due to Y-Chromosome Deletion
Azoospermia
Y Chromosome
In situ hybridization, fluorescence
Hypospadias
Chromosome rearrangement
Biotechnology & applied microbiology
Hypertelorism
Gene probe
Genetics & heredity
Chromosomes, human, pair 1
C banding
Chromosome deletion
Phenotype
Inversion, chromosome
Cleft palate
Chromosomes, human, y
Micrognathia
Human
congenital, hereditary, and neonatal diseases and abnormalities
Centromere
Karyotype
Research & experimental medicine
Pericentric inv(1)
Simiae
Chromosome analysis
Sex chromosome aberrations
Article
Physical examination
Translocation, genetic
Autosome
Case report
Craniofacial abnormalities
Humans
Medicine, research & experimental
Chromosome-1
Male infertility
Y chromosome
Chromosome 1
Frontal bossing
Familial pericentric-inversion
Growth retardation
Newborn
Hammer toe
Infertility
Karyotyping
Reciprocal translocation
Y-autosome translocation
Congenital malformation
Palatopharyngeal incompetence
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Accession number :
- edsair.od......9458..b715a57ff549b4472c0f5ab5a4542b6e