Dermatoglyphic study in children with phenylketonuria
- 1 September 1989
- journal article
- conference paper
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 12 (3) , 323-326
- https://doi.org/10.1007/bf01799225
Abstract
Dermatoglyphic findings in 19 patients with phenylketonuria (11 male and 8 female), 39 of their relatives (18 female and 21 male) and 500 controls (TRC) were not statistically significant among the three groups studied. There was no definite relationship between the phenylketonuric gene and the dermatoglyphic patterns. The parents of half the phenylketonuria cases are not consanguineous; thus the phenylketonuria gene may be more frequent in Turkey than other European countries.This publication has 8 references indexed in Scilit:
- Incidence of phenylketonuria and hyperphenylalaninaemia in a sample of the Turkish newborn populationJournal of Inherited Metabolic Disease, 1986
- Frequency of inborn errors of metabolism, especially PKU, in some representative newborn screening centers around the world: a collaborative study.1975
- Frequency of inborn errors of metabolism, especially PKU, in some representative newborn screening centers around the worldHuman Genetics, 1975
- Dermatoglyphic nomogram for the diagnosis of Down's syndromeThe Journal of Pediatrics, 1970
- The genesis of dermatoglyphicsThe Journal of Pediatrics, 1969
- An information and discriminant analysis of fingerprint patterns pertaining to identification of mongolism and mental retardation.1968
- Dermatoglyphics in phenylketonuriaHuman Genetics, 1967
- Finger, hand and foot prints in phenylketonuria as compared with other normal and abnormal populationsPublished by Springer Nature ,1965