The situations on chromosomes and dermatoglyphics of 19 children with congenital malformation at the Oloppalme hospital
- Author:
Hoan Thi Phan
- Publication Type:Journal Article
- Keywords:
congenital malformation
- MeSH:
Congenital;
Chromosomes;
Dermatoglyphics
- From:Journal of Vietnamese Medicine
2000;254(12):10-17
- CountryViet Nam
- Language:Vietnamese
-
Abstract:
19 children at the age from 2 days to 15 years old includes: 15 females, 3 males and 1 hermaphrodite: - The clinical examinations, health records, analysis of chromosomes and dermatoglyphics shown that : In 5 cases with chromosomal aberrations: + 3 cases down (2: trisomi 21 and 1 down translocation D/G) + 1 case with symtoms of male turn (chromosome Y chromosome F)+1 case hermaphrodite, karyotyp 46, XY, with muti- malformations and female phenotype. -The analysis of acrocentric- chromonomal association shown that: +Frequency of acrocentric- chromosomal associations: 62% + Frequency of acrocentric- chromosomal associations per cell: 1.18. + The means of chromosomal association: 2.13. +Frequencies of gaps, isogaps, chromosomal aberrations, chromatid aberrations are the same in comparision with the other researchers. + In all of three patients with limb malformations, there are abnormalities in dermatoglyphics
