A family study of dermatoglyphic traits in India: resolution of genetic and uterine environmental effects for palmar pattern ridge counts

The inheritance of palmar pattern ridge counts for individual palmar areas, combined distal areas, and all ten areas combined was investigated in families belonging to two strictly endogamous Brahmin castes of peninsular India. Ridge count phenotypes were obtained by the method proposed by Malhotra et al. (1981a), however, zero observations (indicating patterns not circumscribed by triradii) were excluded from analysis. Path analytic methods were applied in order to determine the relative influences of polygenes, intrauterine environment, and residual environment. The proportion of genetic variation was, in general, consistently greater in one population than the other, and significant intrauterine environmental effects were detected for the population with lower heritabilities. The results of this investigation suggest that a simple polygenic model may not be sufficient to explain the inheritance of ridge counts in the interdigital IV configurational area. Distal pattern ridge counts do not appear to be influenced by more or less uterine environmental effects than all areas considered together. The proportion of genetic variation for the total palmar pattern ridge count was 52% in both populations.     

Genetic parameters of dermal patterns of ridge counts.

Dermatoglyphic traits including ridge counts and pattern type counts on fingers were studied in 711 families representing six racial groups in Hawaii. Heritability tesimates were derived from regressions of offspring on father, mother and mid-parent values as well as from full-sib correlations. These estimates varied from 0.23 for radial loops to 0.80 for total ridge count. The heritability estimates were lower for ridge counts of single hands or single digits.     

Path analysis of palmar ridge counts.

The methods for path analysis of family resemblance (Rao et al., '74) are employed to test hypotheses concerning the inheritance of a-b, b-c and c-d palmar ridge counts using the correlation data of Pateria ('74). Homogeneity chi-square tests of the various familial correlations provide no evidence for sex-linkage of either kind, and also suggest that maternal effects are absent. The path coefficient model employed here involves heritability (additive) and common sibling environment. Variance components show that both heritability and common environment are significant, and account for most of the variation at each of the three ridge count area; b-c has the highest heritability, significantly higher than that for a-b or c-d.     

Diversity of palmar pattern ridge counts in Iranian populations

We analyzed bilateral palmar prints of 3,158 individuals from 13 Iranian populations of diverse origins for palmar pattern ridge counts. Right palms did not show greater counts than the left in the majority of the populations studied. Highly significant interpopulational variation was observed for most palmar areas of both males and females. Dendrograms of males and combined sexes showed a good fit with the ethnohistoric background of the populations studied. The results thus demonstrate variation in the palmar pattern ridge counts of populations of diverse origins and may be used as a good measure of population distance.     

Quantitative characterization of finger and palm dermatoglyphics in Bulgarians

In the present paper data on finger and palm ridge counts of both hands are reported from representative samples of healthy Bulgarian males and females. Dermatoglyphic prints from both hands of 2431 Bulgarians (1161 males and 1270 females) have been taken in 116 settlements all over the country. The investigated males and females were healthy, not related persons of Bulgarian origin. The results of finger and palm ridge counts include basic statistics and correlations between ridge counts on separate fingers and the correlations between ridge counts in separate interdigital areas. The results, presented together with data on other dermatoglyphic features elaborated and published till now by the same authors for representative samples of Bulgarian males and females, can serve for the set up of a detailed data basis of the dermatoglyphic status of the Bulgarian population. At the same time they could serve as a norm for clinical and medico-biological investigations with theoretical and scientific applied purposes.     

Genetic basis of a-b,b-c and c-d ridge counts on human soles

The mechanism of inheritance of ridge count of plantar inter-digital areas has been studied among Brahmans of Sagar town of Central India. The correlation coefficient between ridge counts in various family relationships lend support to the concept of an additive genetic model.     

Fixed and random effects in the variation of the finger ridge count: a study of fragile-X families.

A maximum-likelihood scoring technique for analysis of pedigree data allows for the concurrent estimation of random and of fixed effects in a quantitative trait. We included both types of effects in genetic models, to study the sources of variation in finger ridge count in 54 large families affected with the fragile-X disorder. The fixed effects were represented by fragile X and sex, and the random effects by environmental and genetic variance. We found a significant effect of fragile X in the mean of the finger ridge count on the thumb (finger 1) and index finger (finger 2), which had the lowest heritability and a negligible nonadditive component of genetic variance. This was in contrast with ridge counts on fingers 3 and 4, which showed little fragile-X effect, but high heritability and a significant nonadditive component. A contrast in genetic properties for ridge counts on fingers 1 and 2, compared with these counts on the remaining three fingers, may be relevant to increased selection pressures on functions of the thumb and of the index finger in evolution of modern man. We have also demonstrated an important effect of fragile X in increasing the additive variance in covariance, especially between male pairs. These findings suggest that the effect of the fragile-X genotype in finger ridge count is additive and superimposed on the normal hereditary variations in this trait.     

Genetics of epidermal ridge minutiae

Epidermal ridge minutiae have been utilized widely in Forensic Sciences for personal identification for a long time; but genetical significance of minutiae is yet to be understood thoroughly. In the present communication an attempt has been made to study the genetical aspects of finger ridge minutiae on the basis of family material. Data for the present study were collected from 76 families belonging to the Namasudras, a Scheduled Caste residing in Nadia district, West Bengal, India. An eight-fold classification of minutiae was followed in the present study. Out of eight minutiae types ridge end and connecting ridge have shown the maximum and minimum occurrences, respectively. Bilateral difference in minutia types was not evident but the sex difference was found to be significant. The genetics of minutia types was studied by familial correlation (r) and heritability (h ²) estimates. Statistically significant familial correlation values and high heritability estimates for some of the minutia types such as fork, ridge end and total minutiae are suggestive of hereditary control of minutiae. The results of the present study suggest that minutiae showing significant correlation values and high heritability estimates (more than 60%) are useful in genetical studies and perhaps diagnosis of some genetical disorders in addition to their regular application in personal identification.     

Genetic basis of a-b, b-c and c-d ridge counts on human palms

The mechanism of inheritance of ridge count of palmar interdigital areas has been studied among Brahmans of Sagar town of Central India. The correlation coefficients between ridge counts in various family relationships lend support to the concept of an additive genetic model, especially for the b-c or second interdigital area.     

The dermatoglyphics of a Toronto sample of children with XXY,XXYY, and XXX aneuploidies

Dermatoglyphic analyses were carried out on a sample of children with known sex chromosomal aneuploidies (25 XXY, 10 XXX, 1 XXYY). Digital ridge counts and pattern types were determined for each individual. Palm prints and sole patterns were also examined. The results of our study were compared with data from previous studies of sex chromosomal aneuploidies. Our results for the XXY males agree with the findings from other studies with respect to total ridge counts and plantar dermatoglyphics, but not for digital pattern frequencies. Our one example of an XXYY male showed hypothenar patterns similar to those found for this syndrome by other researchers, but neither the digital pattern types nor the unexpectedly high total ridge count conforms to the findings from other studies. Our sample of XXX females falls within the normal XX female range of variation with respect to hypothenar patterns and total ridge count; plantar features show a higher incidence of patterns than previously reported.     

精神分裂症患者皮纹a-b嵴线数波动性不对称的研究

本文分析了精神分裂症患者134例(男性70例,女性64例)和正常对照人群331例(男性170例,女性161例)皮纹a-b嵴线数波动性不对称的分布特征。结果表明:⑴精神分裂症患者双手皮纹a-b嵴线数明显低于正常对照组(P<0.01),表现出明显增高。     

Diversity in palmar pattern ridge counts among 12 Iranian populations

Bilateral palmar prints of 604 male individuals from 12 Iranian groups, six Mongoloid and six Caucasoid, have been analyzed for palmar pattern ridge counts (PPRC). Highly significant variation has been observed in the size of the palmar patterns in all the configurational areas among the Iranian groups. The distance analysis based on PPRCs differentiated the Iranian Mongoloid from the Iranian Caucasoid groups into distinct clusters. The pattern of differentiation based on PPRCs explained the ethnohistoric relationships between the Iranian groups as well as between the Iranian and the 20 Caucasoid groups from India much better than the palmar pattern frequencies. The results of this study demonstrate the existence of variation in the size of the palmar patterns across different populations within an ethnic group, as well as that among different ethnic groups, and seems to be a better indicator of interpopulational diversity than the palmar pattern frequencies.     

A family study of dermatoglyphic traits in India: a search for major gene effects on palmar pattern ridge counts

Palmar pattern ridge counts were subjected to segregation analysis in an attempt to identify possible major gene effects on these dermatoglyphic traits. The phenotypes considered were total palmar pattern ridge count, and ridge counts for the right interdigital III and IV and left interdigital IV individual palmar areas (sample sizes were too small for the other palmar areas). Evidence of familial resemblance was found for all of the phenotypes studied, and initial evidence for a major effect was found for all but the right palm interdigital III ridge count. However, this initial evidence could be attributed to nongenetic effects in each case, including skewness in the trait distribution. Tests for agreement with Mendelian transmission frequencies were found to be very useful in discriminating between a non-Mendelian major effect and a major gene. We concluded against a major gene effect for any of these traits, and multifactorial inheritance remains a plausible alternative explanation for the familial resemblance.     

Estimating heritability using family-pooled phenotypic and genotypic data: a simulation study applied to aquaculture

Estimating heritability based on individual phenotypic and genotypic measurements can be expensive and labour-intensive in commercial aquaculture breeding. Here, the feasibility of estimating heritability using within-family means of phenotypes and allelic frequencies was investigated. Different numbers of full-sib families and family sizes across ten generations with phenotypic and genotypic information on 10 K SNPs were analysed in ten replicates. Three scenarios, representing differing numbers of pools per family (one, two and five) were considered. The results showed that using one pool per family did not reliably estimate the heritability of family means. Using simulation parameters appropriate for aquaculture, at least 200 families of 60 progeny per family divided equally in two pools per family was required to estimate the heritability of family means effectively. Although application of five pools generated more within- and between- family relationships, it reduced the number of individuals per pool and increased within-family residual variation, hence, decreased the heritability of family means. Moreover, increasing the size of pools resulted in increasing the heritability of family means towards one. In addition, heritability of family mean estimates were higher than family heritabilities obtained from Falconer’s formula due to lower intraclass correlation estimate compared to the coefficient of relationship.Subject terms: Genome evolution     

Fingerprint pattern factors

Factor analysis was employed using the ulnar ridge count, radial ridge count, ridge count (the larger of the radial or ulnar count as generally used for calculating total ridge count), and pattern type for each finger in 720 twins. Pattern type and ulnar count displayed parallel factor loadings while loadings for radial and ridge count also paralleled each other. This relationship did not hold for the index finger, indicating the importance of pattern direction and greater pattern diversity for this digit. Total ridge count was most closely associated with a factor of ring and little finger radial and ridge count and only secondarily with an index finger factor. When radial and ulnar counts were deleted to make comparisons with earlier studies, the result was factors having groupings of variables identical with previous reports. It appears that factor analysis results in consistent extraction of identical or very similar factors from different populations, and the use of radial and ulnar counts adds more information than when only the larger of the two counts is considered.     

Ridge counts of plantar dermatoglyphic interdigital areas and the relation of their trends to the anatomical axis

Brahman and Bhangi, two endogamous groups of Hindu society, have been studied for ridge counts of plantar interdigital areas. No significant sexual difference, excepting a–b ridge count for Brahmans, was observed. Similarly, nonsignificant bilateral variation is exhibited. No ethnic variation is observed as regards the mean total a–b, b–c and c–d counts. The distribution of ridge counts can be correlated with the anatomical axis of the palm and sole. The palm (Pateria, '67) shows the minimum value for b–c and the sole for a–b. Therefore the minimal counts coincide with anatomical axes, corresponding to the common localization of syndactyly.     

Dermatoglyphic analysis in bipolar affective disorder and schizophrenia--"continuum of psychosis" hypothesis corroborated?

Dermatoglyphic features are thought to be indicators of events in the early embryonal stages. They might also be associated with the developmental disorders of the central nervous system (CNS) including schizophrenia. Dermatoglyphic features of 92 male patients with bipolar affective disorder (BPAD) (unipolar depression and schizoaffective psychosis were excluded from the study) were compared with those of 195 males with schizophrenia (SCH) and both with those of 200 male controls (control group-CG). DSM-III-R criteria were used for the diagnostic evaluation. Quantitative analysis showed only one statistically significant difference between BPAD and SCH patients groups, regarding the c-d ridge count of the left hand. The canonical discriminant analysis did not permit correct classification (only 59.23% of cases were correctly classified) between BPAD and SCH. Numerous quantitative dermatoglyphic features of both BPAD and SCH differed significantly from those of the control subjects. Finger ridge counts as well as palmar ridge counts were markedly lower in BPAD and SCH as compared to the controls. These findings are not in contradiction with the hypothesis claiming that psychoses are a set of diverse expressions (due also to noninherited factors) of a single underlying entity.     

Cusp size, sexual dimorphism, and heritability of cusp size in twins.

Overall measures of mandibular molars reflect the combined size contributions of the component cusps and ridges. Until now, the size hierarchy of primary and permanent mandibular molar cusps remained unclear. This paper utilizes the relative plane surface areas (basal area dimensions) of the individual molar cusps, as assays of cusp size to demonstrate cusp size variations within populations, antimere cuspal variations, sexual dimorphism, and, the heritability of cusp size. Duplicate dental casts from 199 pairs of like-sexed twins provide the raw dats. Defined anatomic landmarks on the occlusal surfaces were reduced to X-Y rectangular coordinates prior to the computation of the basal areas dimensions. The results establish a cusp size hierarchy specific for molar type, i.e., five-cusped molars with a distal fovea and distal marginal ridge (5fd), five-cusped molars without a distal fovea and without a distal marginal ridge (5o), and four-cusped molars (4c). Sexual dimorphism in cusp size is apparent in 5fd molar cusped but not in 5o molar cusps. However, males have a significantly higher frequency of 5fd molars. Females have a higher frequency of smaller 5o and 4c molars which have fewer crown components. Moreover, female 5o molars have cusps as large as or larger than 5o male molor cusps. Right-side-left-side differences exist between antimere cusps based on relatively low correlations. The mirroring of molor types occurs infrequently. When observed, most intrapair differences for cusp size, using F-ratios, indicate a low component of hereditary variability.     

中国延边朝鲜族手皮纹研究

本文观察研究了400例（男200例;女200例）中国延边地区朝鲜族手的皮纹。调查分析了指纹类型、指嵴纹计数与总数、a-b嵴纹、掌纹真实花样百分率、掌纹类型、atd角等项系数。进行了不同性别、不同民族和人种间的差异性比较。结果表明朝鲜族手皮纹有一定的特征。     

Quantitative digital dermatoglyphics in males and females of four Sardinian linguistic groups

Radial and ulnar ridge counts on each of the 10 fingers, total finger ridge count, bilateral summed radial and ulnar finger ridge counts, an index of asymmetry between homologous fingers and two indices of intraindividual diversity of finger ridge counts were used to identify biological relationships among Sardinian linguistic groups. Stepwise discriminant analysis of 26 digital traits of 1258 Sardinians, 647 females and 611 males, was carried out. The results indicate high intergroup heterogeneity; moreover, with p≤0.01 as F-to-enter and p≤0.05 as F-to-remove, only 5 of the 26 digital variables are in the model (URC R5, RRC L5, RRC R5, URC R4, URC L5). The pattern of interpopulation biological relationships shows a clearly distinct position of the Gallurian group (both males and females), which speaks an Italian dialect. It originated mainly from Corsican immigration to the Gallura region starting from the XVII century. While the properly Sardinian linguistic groups (Campidanian and Logudorian) and the Sassarian group, which speaks an Italian dialect that developed as a “lingua franca” during the Middle Ages (XII–XIV centuries) due to linguistic contact between Sardinians and Italians, are positioned close to one another. This pattern agrees more with the ethno-historical back-ground than with the linguistic one.