The frequency of fingerprint type in parents of children with Trisomy 21 in Japan

Analysis of the frequency data of each fingerprint type (arch, ulnar loop, radial loop, and whorl) of the parents of children with Trisomy 21 (Fathers: 71; Mothers: 128) born between 1965 and 1970 obtained from the Tokyo Medical and Dental University Hospital was carried out. Japanese controls were taken from dermatoglyphics data in Japan. We conducted the Friedman test on each type of fingerprint between Japanese controls and parents of Trisomy 21 children.Results from a statistical analysis based on the above data showed significant differences, more arches (p < 0.0001) and fewer whorls (p < 0.05) in mothers of children with Trisomy 21. Among fathers of Trisomy 21 children, a significant difference was found in there being fewer whorls (p < 0.05) and ulnar loops (p = 0.06). Considering the mothers' fingerprints, we suspected that females with a higher frequency of arches and a lower frequency of whorls had a stronger possibility of bearing Trisomy 21 babies. On the other hand, in fathers of Trisomy 21 children, we considered that there would be a possibility of significant differences if cases in the sample were increased.     

Viability of beta-thalassemia hetero- and homozygotes in several populations of Central Asia]

Viability of hetero- and homozygotes for beta-thalassemia was studied in two isolated populations born after 1950 in conditions of malaria absence. Pregnancy outcomes and probability to get 16 years old were compared in marriages, in which one or both parents were heterozygous for beta-thalassemia, and in marriages, with both parents being normal. The ratio of children with normal genotype and children heterozygous for beta-thalassemia in families, where one parent was heterozygous for beta-thalassemia. Preliminary conclusions are made on the basis of the data obtained. Viability of children in families where one parent is heterozygous for beta-thalassemia is found to decrease in the absence of selective factors (malaria) as compared with normal children. The highest viability decrease was observed in the progeny of those families where both parents were heterozygous beta-thalassemia. Elimination mainly takes place within the first year of life.     

Dermatoglyphics of the relatives of children with congenital defects in development]

The localization of an axial triradius and the flexor creases were studied in 173 phenotypically normal mothers and 104 fathers of congenitally malformed children. The most pronounced changes ofdermatoglyphics were found in the parents of children with polygenic determined defects, less pronounced ones-- in the parents of children with multiple congenital non-chromosomal defects and with Down's syndrome. The frequency of the pathological features studied was similar both in children with polygenically determined isolated defects and with Down's syndrome. The frequency of the pathological determined isolated defects and in their parents. In multiple congenital defects and in Down's syndrome the abnormalities ofof the localization of an axial triradius and of the flexor creases were found in children more frequently than in the parents. It is suggested that the above mentioned peculiarities of parental dermatoglyphics may be useful for the genetic counsleling.     

210例糖尿病患者的皮纹学研究

本文报告了210例糖尿病患者皮纹的11个参数,与对照组相比,各型男患者的足底(足母)趾球区纹型中,三角斗形纹均显著增多;NIDDM型男女患者atd角显著变小;NIDDM型女患者通贯手出现率显著增高;NIDDM型女患者主线C走向I_3的百分率显著增高;各型女患者的指纹中斗形纹出现率显著增高,而尺箕著减少。     

Prenatal diagnosis of inherited hemoglobinopathies

In this paper we reviewed the different methods presently available for prenatal diagnosis of hemoglobin disorders and the impact of this technology in the control of beta-thalassemia in several Mediterranean populations. The vast majority of the inherited hemoglobinopathies can now be detected in the fetus by amniocyte or trophoblast DNA analysis. alpha-thalassemias, delta beta-thalassemias and gamma delta beta-thalassemias, which are usually caused by a gross structural rearrangement of the DNA, may be directly detected by Southern blot analysis. Only a few beta-thalassemia lesions are caused by gene deletion or affect a restriction recognition site and thus may be directly identified by this method. The major part of beta-thalassemia are due to single nucleotide substitution, small deletion or addition which do not alter a restriction recognition site. These mutations may be directly detected by complementary oligonucleotide probes. Alternatively, when normal or affected children are available, fetal diagnosis may be accomplished by linkage analysis with polymorphic restriction sites. Fetal blood analysis is used at present time for those cases presenting too late in the pregnancy for characterization of the molecular defect and in prospective parents in whom the defect is not known. Introduction of prenatal diagnosis in combination with carrier screening in several mediterranean populations led to a consistent reduction in the incidence of homozygous beta-thalassemia.     

Dermatoglyphics in pathology with emphasis on breast cancer and cervix carcinoma: Some results

The finger and palmar prints of 118 women with breast cancer and of 37 women with cervix carcinamo were studied. The results were compared with two groups of healthy women, the first consisted of aged women (average age of 78.94) and the second of young women. Only four differences out of ten (40%) were significant between women with breast cancer and young women. One difference out of ten (10%) was significant in the comparison between women with carcinoma of the cervix and elderly women and two (20%) in the comparison to young women. In general, compared with the healthy women the sick women present an increase in whorls and a decrease in a-b ridge count. The results obtained seem to demonstrate that dermatoglyphics are not a good diagnostic tool in the study of these two types of cancer.     

Quantitative and qualitative finger dermatoglyphics in the Basque Valley of Urola, Spain

Digital dermatoglyphics of an indigenous sample of 87 males and 101 females from the Urola Valley in the Spanish Basque Country are compared with those from the nine other Basque valleys previously analyzed. In both sexes of the Urola Valley, there is a very high frequency of radial loops; the mean found in this valley extends the range of variation for South European-Mediterranean populations, and it is in the superior limit of all Caucasian populations. There are bimanual and sex differences in the frequencies of whorls and loops. Contrary to what occurs normally in populations, in the Urola Valley the frequency of whorls is higher in females and the quantitative value of digital patterns is lower in males. The results of this study show the existence of heterogeneity among valleys for digital trait frequencies and for finger ridge count, and this heterogeneity is more marked in females.     

Finger dermatoglyphics and their asymmetry in Bulgarian right-, mixed- and left-handers

Since Bulgarians have never been investigated concerning the relationship between handedness and dermatoglyphics, the present study was aimed to investigate the aforementioned relationship in a Bulgarian sample. Digital dermatoglyphics and their asymmetries have been studied in 870 apparently healthy students from randomly selected Bulgarian secondary schools: 264 right-handers (RH), 246 mixed-handers (MH) and 360 left-handers (LH). The whorls were significantly less frequent and the ulnar loops more frequent in RH than in the other two handedness categories. Right-handers exceeded significantly MH and LH in the ulnar fluctuating asymmetries of the first and the fourth finger pairs. As compared to the number of investigated variables and especially to the important psychological and behavioral differences between handedness categories reported earlier in the same sample, the presented significant findings are rather scarce. Nevertheless they could contribute to the accumulation of data concerning the investigated relationship and to its better understanding.     

The dermatoglyphics of the Elema people from the Gulf district of Papua New Guinea

The present report deals with the digital and palmar dermatoglyphics of the Elema peoples from the Gulf District of Papua New Guinea. The samples involved 91 males and 134 females from the areas of Iokea, Sepoe and Karama. The Elema dermatoglyphics, compared to those of other peoples in New Guinea, were found to have a high pattern intensity index and frequency of whorls, and the highest frequency of ulnar type C line, complete simian creases and patterns in the IV interdigital areas of the palms. On the other hand, their 11/7 ratio of the D line, the main line index, and the frequencies of patterns in the hypothenar, thenar/I and II interdigital areas were lower than most other groups on the island; they also have the lowest R/U ratio. All dermatoglyphic features considered, the frequencies in the Elema group were for the most part found to be near the extremes of the range of the dermatoglyphic frequency distributions in New Guinea populations. The dermatoglyphic distributions of New Guinea as a whole are discussed in terms of those of the other Australasian populations with comments on the dermatoglyphic comparisons between the Australasians and the other major human groups, Amerindians, Orientals, Asian Indians, Caucasians and Negroes.     

Palmar dermatoglyphics in mental retardation

Palmar dermatoglyphics has been studied in 86 mentally retarded males versus 50 normal males. The important findings in brief are as follows:

1. Frequency of patterns in descending order (all ten taken together) were ulnar loops followed by whorls, in both the groups.
2. Highly significant differences were found between the two groups in righ c-d, a-d, left a-b, a-d and vertical distance from a-d to the axial triradius, significant differences in left b-d, c-d and both distances from axial triradius to a vertical dropped proximally from triradius a.

The finding of this work has been compared with other authors. These findings give a base to classify mental retardation from the dermatoglyphic point of view, thus to help in diagnosis of the disease in newly born individuals.     

Dermatoglyphics in childhood leukemia

The dermatoglyphics of 54 leukemic children do not differ significantly from those of 25 mothers and 592 unrelated controls with respect to frequency of digital pattern types, position of axial triradius, or type of palmar flexion creases. These findings do not support the hypothesis that children with leukemia have an increased frequency of unusual dermal patterns, but suggest that the dermatoglyphics of leukemic children are not distinctive and therefore have no practical value in the diagnosis of childhood leukemia. Whatever factors are responsible for the development of leukemia in children, these factors do not appear regularly to affect the differentiation of the dermal ridges.     

Sea-blue histiocytosis and beta-thalassemia in the same family.

Among 5 families with SBH of Neapolitan origin, herediatry glyco-lipidosis was accompanied in one by beta-thalassemia. All 10 members of this family, namely parents and 8 siblings, were investigated. The mother and two children were found to be carriers of both SBH and beta-thalassemia, while three other siblings were carriers of SBH alone. None of the six patients conformed the classic clinical picture often observed in genotypical SBH. The present state of genotypic transmission of the stigma is discussed on the basis of the author's experience as well as the data in the literature. As for the combination SBH-thalassemia in the same individual it may be concluded that the two genes are most likely independent and certainly not linked.     

Digital dermatoglyphics of 107 Bengalis.

I analyzed the finger prints of 59 male and 48 female unrelated Bengalis in a rehabilitation camp of Dacca, Bangladesh. The most common pattern type in the Bengalis was the ulnar loop (53%), then whorls (40%); arches (5%) and radial loops (2%) were the least common. Radial loops occurred most frequently on the index fingers. I have shown the arch/whorl, whorl/loop, and pattern intensity indices, and I have presented ridge counts by individual digits and by total digital ridge count. Digital dermatoglyphics in the male Bangladeshis were similar to previous findings in male Brahmins of Bengal. However, there were more whorls and arches, fewer loops, and a higher mean total digital ridge count in the female Bangladeshis than in female Brahmins.     

Reproductive patterns and thalassaemia major

This study investigated the effect of the diagnosis of transfusion-dependent homozygous beta-thalassemia on subsequent parental reproductive patterns in 44 families in New South Wales. The results indicate a shift over time from parental risk-taking (either consciously or in ignorance of the implications of the diagnosis) to premature curtailment of reproduction to the likelihood of attaining birth expectations through antenatal diagnosis. 67% of families with both of their 1st 2 children affected by thalassemia major had additional children, compared with 38% of those where the 1st child was affected and the 2nd child was unaffected and 37% of families where the 1st child was unaffected and the 2nd child was affected. Overall, 48% of mothers of children with thalassemia major had as many children as they had expected at the time of marriage, 13% had more, and 39% had fewer children. The mothers of older children were less likely to have had the planned number of births than those of children born more recently. The value of antenatal diagnosis to couples at risk of thalassemia appears to have been to enable them to meet or almost meet their birth expectations.     

Does there exist a correlation between the number of whorls of the finger tips and birth order of sibs? (author's transl)]

It was stated by Birdsong and Rashad (1972) that the child of birth order number six of Korean families has significantly more true whorls on the finger tips than older brothers and sisters. To verify this assertion we studied a sample of all members of 43 normal German families with 5 or more legitimate children. The findings of the epidermal finger pattern types and those of the toe patterns were analysed. Results indicate a different conclusion regarding the number of digital whorls which were not increased statistically with increasing number of sibs. The number of whorls were randomly distributed within the heritable range of variability of the particular family. It appears of importance that, due to our analyses, the value of information of the characteristic "number of whorls" is not reduced and does not require a specific consideration regarding birth order. Furthermore, it can be stated preliminarly that there is no hint pointing to an influence of the maternal age on the number of whorls in their offspring.     

Unusual Dermatoglyphic Findings Associated with Cytomegalic Inclusion Disease of Infancy—First Report and Practical Review

Infection with the human cytomegalovirus has a teratogenic effect on the fetus during the first trimester of gestation as does rubella. Since unusual dermatoglyphic findings have been observed in infants with congenital rubella infection, the present study was designed to determine whether or not unusual dermatoglyphics occur in patients with cytomegalic inclusion disease of infancy. Analysis of dermatoglyphics in 15 infants with cytomegalic inclusion disease revealed unusual features in all infants. These features are reported here for the first time and are compared with dermatoglyphic findings in a normal population as well as with those of available parents of the infants.     

Ethnic diversity in Punjab as based on finger dermatoglyphics

Four ethnic groups of Punjab having same dialect viz. Khatris, Jats, Brahmins and Muslims were taken to see ethnic differences in regards to the distribution of whorls, loops, and arches of finger dermatoglyphics. The results show that there is a great diversity in the four groups for these parameters. These groups were compared with similar ethnic groups of other places having different dialect. The results reveal that there seems to be ethnic affinity between the group known by same name and which is true for all the four groups.     

A female infant with monosomy 21

Summary A female infant with total monosomy 21 identified by Q banding is described. The main clinical features were hypertonia, prominent occiput, hypertelorism, antimongoloid slant of the eyes, broad nose, antimongoloid character of dermatoglyphics. Both parents are phenotypically as well as karyotypically normal.     

Geographical variation of digital dermatoglyphics in Africa

Data from 142 male and 43 female samples of African populations have been used to analyze the geographical variation of digital dermatoglyphics (arches, loops, whorls, and pattern intensity index) in Africa. The patterns of geographical variation have been summarized as contours of sixth-degree polynomial surfaces by means of trend-surface analysis. As pointed out by early studies, Africa exhibits geographical clines of digital dermatoglyphic patterns. However, only some of the frequency gradients previously described for the region find confirmation in the present study.     

Surviving social assistance: 12-month prevalence of depression in sole-support parents receiving social assistance

BACKGROUND: Although it is generally recognized that poverty and depression can coexist among single parents receiving social assistance, there is insufficient research on this topic. The goals of this study therefore were to investigate the prevalence, correlates and health care expenditures associated with depression among sole-support parents receiving social assistance. METHODS: Sole-support parents who had applied for social assistance in 2 regions of southwestern Ontario were included in the study. Depression was diagnosed with the 1994 University of Michigan Composite International Diagnostic Interview short forms. RESULTS: The 12-month prevalence rate of depressive disorder among the parents interviewed was 45.4% (345/760). A total of 247 (32.5%) had major depressive disorder alone, 19 (2.5%) had dysthymia, and 79 (10.4%) had both major depressive disorder and dysthymia ("double depression"). Those with major depressive disorder, particularly double depression, had significantly higher rates of coexisting psychiatric disorder than those without depressive disorders. Parents with depression reported higher rates of developmental delay and behaviour problems in their children than parents without depression. Expenditures for health care services were higher for parents with depression and for their children than for parents without depressive disorder and their children. INTERPRETATION: Single parents receiving social assistance have high rates of depression. Such parents with depression also have higher rates of other psychiatric disorders and higher expenditures for health care services, and their children have higher rates of developmental delay and behaviour problems.