Partial trisomy of chromosome 10 inherited from a carrier father.
Indian J Pediatr
;
1995 Sep-Oct; 62(5): 615-8
Article
in English
| IMSEAR
| ID: sea-80991
ABSTRACT
Partial trisomy of chromosome 10q is a very rare condition with only four cases having been reported int he literature. This report describes a neonate with symmetric growth retardation and multiple dysmorphic features, in whom G-banded chromosomal analysis revealed a partial trisomy of chromosome 10q (q2.4-q ter). The father was diagnosed as a carrier of a balanced translocation with a karyotype of 46, XY t(10.3) (q2.4L pter). In patients with a bad obstetric history, genetic counselling prior to a new conception cna aid in early prenatal diagnosis of fetuses with recurrent chromosomal abnormalities by means of fetal tissue sampling.
Full text:
Available
Index:
IMSEAR (South-East Asia)
Main subject:
Pedigree
/
Trisomy
/
Chromosomes, Human, Pair 10
/
Female
/
Humans
/
Infant, Newborn
/
Pregnancy
/
Ultrasonography, Prenatal
/
Chromosome Banding
/
Adult
Type of study:
Diagnostic study
Language:
English
Journal:
Indian J Pediatr
Year:
1995
Type:
Article
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