Dermatoglyphic patterns and pattern intensities of the genus Cacajao (Cebidae,platyrrhini) with observations on interspecific and subspecific differentiation

Palmar and plantar dermatoglyphic pattern types, area and total pattern intensities (API and TPI), and pattern intensity (PI) profiles are presented for the South American genus Cacajao of the subfamily Pitheciinae. The data are based on prints from 41 bald-head uacaries (C. calvus), 9 white bald-head uacaries (C. c. calvus), and 15 black-head uacaries (C. melanocephalus). In each extremity, loops of differing orientation were the most frequent pattern type; whorls were dominant at palmar interdigital (I) area 3 in C. calvus and at both I3 and I4 in C. melanocephalus. Open fields characterized the palmar thenar and plantar proximal hypothenar, thenar, calcar, and I3 and I4. There was little evidence of significant sexual dimorphism as assessed from PI values. The genus displayed significant asymmetry at palmar I3 (P?0.001) and plantar distal hypothenar (P?0.004). There were significant group differences between C. calvus and C. c. calvus in the palmar thenar API and plantar TPIs. The combined bald-head sample of C. calvus and C. c. calvus differed from C. melanocephalus in API of palmar I4 and plantar distal thenar, I2, and distal hypothenar (marginally), and in plantar TPIs. In PI profiles, C. melanocephalus departed from the pattern shared by C. calvus and C. c. calvus in both palmar and plantar interdigital areas. As a genus, the uacaries have markedly low plantar TPI values relative to palmar values (palm-sole index > 195). Of eight comparison cebid genera, only Chiropotes, another pitheciine genus, approximated these values.     

Palmar and plantar pads and flexion creases of genetic polydactyly mice (Pdn)

Attempts to gain a better understanding of the relationship between the epidermal ridge patterns (dermatoglyphics) and flexion creases on the volar aspects of human hands and feet and specific medical disorders led to a search for a suitable animal model, allowing studies of the fetal development of the pertinent structures. A common experimental animal, the rat (Rattus norvegicus), was found to be an excellent candidate, owing to the strong resemblance of the volar pads and flexion creases on its palmar and plantar surfaces to those of human subjects. A hereditary preaxial polydactyly mouse (Pdn) provides an opportunity to study the effects of this malformation on the surrounding morphological structures and, specifically, on the volar pads, i.e., the sites over which the dermatoglyphic patterns develop. The hands and feet of the wild‐type (+/+) mice show no anomalies, and their major pad and flexion crease configurations correspond to those of normal rats. The heterozygous (Pdn/+) mice, in spite of having a thumb/big toe with a duplicated distal phalanx on their hands/feet, did not display any alterations in palmar/plantar pads. The homozygous (Pdn/Pdn) mice have a protrusion in the thenar area and one to three supernumerary digits on the preaxial portion of both the hands and feet. The effect of these anomalies was found to be limited to the pad and flexion crease configurations in the preaxial areas; the postaxial sites were not affected. The original number of pads on the thenar/first interdigital areas of Pdn/Pdn mice was apparently identical to that of the +/+ and Pdn/+ mice. The preaxial protrusion, however, affected the number, size, and location of the pads observed in the newborn mice, resulting in varying pad configurations, such as fused and scattered pads or a pad cluster formed by gathering the neighboring pads. These pad modifications were induced by the preaxial plantar/palmar protrusion only and were not affected by the presence of supernumerary preaxial digits. In view of the similarities in the morphology and fetal development of human and mouse distal limbs, the present study is relevant to human subjects, particularly to the understanding of the significance of dermatoglyphic variations in individuals with specific medical disorders. Future studies of naturally occurring or experimentally induced limb malformations in mice or rats should provide valuable insights into the development of human hands and feet and into factors contributing to their congenital anomalies. J. Morphol. 239:87–96, 1999. © 1999 Wiley‐Liss, Inc.     

Palmar flexion creases and dermatoglyphics among diabetic patients

Palmar dermatoglyphics and flexion creases of 108 male and 65 female patients diagnosed as having diabetes mellitus have been analysed. The control population consists of 536 males and 234 females from the same population. Palmar flexion creases were analysed according to the method suggested by Bali and Chaube ('71). The flexion creases of diabetic patients and the control population are significantly different. The differences between main line formulae in diabetes and controls are significant among males. The differences between C-line types of patients and controls are significant among both sexes. Axial triradii are significant among female patients and controls. The patterns in the interdigital areas IV and II are significantly lower among male and female patients respectively from their controls.     

Palmar dermatoglyphics in different phenotypic manifestations of schizophrenia]

Palmar dermatoglyphics was studied in 1120 patients with schizophrenia with due regard for its form, and in 1240 healthy persons of the same population. The frequency of the AU/AC type of patterns in the hypothenar area was increased in women with schizophrenia and its paranoid form. Among men with schizophrenia and its simple form the frequency of dysplasia, true and defective patterns on the thenar was increased; in addition in men with the paranoid form the frequency of loops in the 3d interdigital areas was also increased.     

Palmar pattern frequencies as indicators of relationships among Sardinian linguistic groups of males

Palmar pattern frequencies were used to calculate distance coefficients between Sardinian linguistic groups of males for the purpose of verifying, by means of correlation matrix analyses, whether or not the dermatoglyphic traits considered lead to a reliable identification of the biological relationships on the basis of the linguistic backgrounds of these groups. With Sanghvi's as the distance measure and by using palmar pattern frequencies in the Hy area, Th/I, II, III, and IV interdigital areas and all traits together for palms combined or separated were calculated dermatoglyphic distance measures. Mantel tests of matrix correspondence showed that, by using palmar pattern frequencies in the Th/I interdigital area (palms combined), in the II, III, and IV interdigital areas, or all traits together for palms combined and separated, statistical significance between dermatoglyphic and linguistic distances can be obtained, even when the effect of geography is removed; there is no statistically significant correspondence between geographic and dermatoglyphic distance matrices, even when the effect of language is removed. The results obtained in this study by means of the Mantel test procedure demonstrate that the dermatoglyphic traits analyzed, with the exception of palmar pattern frequencies in the Hy area and in the Th/I interdigital area for plams separated when these areas are used singly, can be considered as a good set of variables to use in finding biological relationships between Sardinian linguistic groups of males examined on the basis of their linguistic backgrounds.     

Palmar and plantar pads and flexion creases of the rat (Rattus norvegicus)

The recent detection of dermal ridge configurations on the volar pads of the rat (Rattus norvegicus) has created opportunities for experimental studies of dermatoglyphics. In the present work, the palmar and plantar surfaces of the rat were studied to establish the feasibility of comparative rat and human dermatoglyphic investigations. The studied features included the volar pads and flexion creases. The number and location of the palmar and plantar pads in the rat were found to be similar to those of humans. The exception was a previously unrecognized small pad on the palms and soles of the rat, located on the radial and tibial side, respectively, of the proximal component of the first interdigital pad. This pad has no parallel in human embryos. Rats were found to have flexion creases in the non-pad areas between the neighboring pads, similar in location and appearance to those of humans. Unlike humans, however, rats also have boundary creases, separating the pad and non-pad areas. The marked similarities in the morphology of the volar areas between rats and humans make the rat ideally suitable for experimental studies of dermatoglyphics and flexion creases. Results of such studies should be applicable to human developmental dermatoglyphics, including those pertaining to medical disorders. © 1994 Wiley-Liss, Inc.     

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.     

一千例甘南藏族手纹学分析

本文报道1000例甘南藏族手纹学正常值。各类指端纹型按出现频率的多少依次为:尺箕(Lu)、斗形(W)、双箕(Wd)、桡箕(Lr)、弓形(A)、帐弓(A~t)。掌褶正常型占74.45±0.97、通贯手占8.15±0.61、总指嵴数168.10±51.54、a—b嵴数34.95±8.92、atd角(度)39.18±4.36。     

Toe and plantar dermatoglyphics in adult American Caucasians

The scarcity of information on control data of toe and plantar dermatoglyphics led us to undertake this study of adult American Caucasians. Toe and sole prints of 168 male and 83 female participants of the Baltimore Longitudinal Study of Aging were analyzed. Toe pattern frequencies demonstrate that fibular loops are the most prevalent pattern on the toes in both males and females. Pattern distribution by digit shows that arches are most often located on the fifth toe while whorls are found with greatest frequency on the third toe. Plantar pattern frequencies indicate that the most common pattern found in the hallucal area is the distal loop. Open fields are frequently found in the II and IV interdigital areas while distal loops are prevalent in the III area. These results are compared to the finger and palmar patterns of the same individuals. The distribution of patterns on the toes and fingers of the same individuals appear to be quite different. Population comparisons did not demonstrate a clear racial difference in the toe pattern frequencies or in the plantar areas.     

The dermatoglyphic and clinical features of the 9p trisomy and partial 9p monosomy syndromes

Summary The physical and dermatoglyphic features obtained from published reports of 128 patients with the trisomy 9p syndrome and 27 patients with the partial 9p monosomy syndrome are tabulated. This information is also provided on two new individuals with each of these chromosomal disorders. The dermal ridge patterns and palmar creases of trisomy 9p which are most helpful from a diagnostic standpoint are zygodactylous or absent palmar digital triradii, brachymesophalangy, reduced total finger ridge count, complex thenar/ID I patterns, transverse palmar ridge alignment, simian creases, distal axial triradii, and great toe and hallucal arch patterns. The characteristic features in partial 9p monosomy include dolichomesophalangy with accessory finger flexion creases, digital whorl patterns and elevated total finger ridge count, distal axial triradii, simian creases, and palmar dermal ridge dissociation.     

Dermatoglyphic peculiarities in patients with hypomelanosis of Ito (Incontinentia pigmenti achromians). A new case

We have analyzed the dermatoglyphic aspects of a patient affected by hypomelanosis of Ito (Incontinentia pigmenti achromians — HI) and of his healthy mother, and have compared our findings with those of the only three other cases in whom such studies had been done. It appeared that hypomelanosis of Ito shows anomalous dermatoglyphic peculiarities: a larger number of ulnar loops and the frequent absence of patterns in thenar, II and III interdigital areas. However, the absence of some interdigital triradii, particularly of d triradius, seems to be the most distinctive character. Since the timing of embryonal life during which d triradius should be formed is between 16 and 17 weeks, it seems highly probable that some developmental abnormality might occur at this point in HI. Moreover, the present analysis allows to support some hypotheses already proposed in the literature, concerning the modalities of determination of the absence of d triradius. The observed concomitance with some dermatoglyphic findings, such as the absence of other palmar triradii and the absence of interdigital patterns, led us to suggest that such characteristics could be connected each other, having perhaps a common genetical basis or undergoing the same microenvironmental effects.     

Palmar flexion creases in schizophrenia

Palmar flexion creases have been studied in schizophrenics with a family history of schizophrenia or other psychiatric disorders and without such a background, and compared to a control population. Palmar flexion creases have been analyzed according to the method suggested byBali & Chaube (1971). When compared to controls, differences in the DRBC and TRBC frequencies are significant in the subgroup with no family history, supporting the existence of biological heterogeneity in schizophrenia, and of congenital factors when there is no known genetic background.     

Qualitative aspects of palmar dermatoglyphics in a sample of Sardinian population

The author examines certain qualitative aspects of palmar dermatoglyphics in 820 individuals of both sexes from the city of Cagliari (Sardinia). The overall results obtained are discussed and the sexual and lateral differences are considered. The sample examined differs from other Mediterranean samples because of a tendency toward a vertical trend of the papillary lines, a lower frequency of patterns in the 2nd and 3rd interdigital areas and a higher frequency of patterns in the 4th interdigital area.     

裕固族皮纹学初步研究

本文研究了甘肃裕固族青少年儿童346人的皮纹学特征,报道了斗、箕、弓各型指纹的频率,指纹指数,总指嵴数,a-b嵴数,通关手出现率,掌纹真实花样等8项皮纹学参数和主线止区的分布比例。并作了性别、手别、族别及人种间的比较。结果表明,裕固族既具有蒙古人种的皮纹特征,也有一些白种人的皮纹特点,这可能暗示着裕固族有白种人的血统。     

Dermatoglyphic changes in human genetic disorders: preaxial defects of the upper limbs]

Dermatologlyphic prints of 9 patients with preaxial (radial) hand defects were compared with control ones. A correspondence is revealed between a decrease in thumb phalanx length and a respective decrease in ridge count, on the one hand, and between the 1st metacarpal hypo- or aplasia and a decrease in palmar ridge count between the metacarpo-phalangeal and thumb flexion creases, on the other hand. An interrelation is found between the anomalies in flexion crease and respective joint formation. It is suggested, that these disorders are due to genetically determined anomalies in morphogenetic gradients which control the distribution of positional information in upper limb morphogenetic field.     

Hemochromatosis gene sequence deviations in German patients with porphyria cutanea tarda

Patients with porphyria cutanea tarda (PCT) reveal a susceptibility to reversible inactivation of hepatic uroporphyrinogen decarboxylase, which might be triggered by alcohol, hepatitis C virus infection, and iron overload. Inherited factors that may predispose to clinically overt PCT also include sequence deviations in the HFE gene that is mutated in classical hemochromatosis. Here, we studied the prevalence of both common and rare hemochromatosis gene variations in 51 PCT patients and 54 healthy controls of German origin. The frequency of the common HFE gene mutation C282Y was 15.7 % in PCT patients and 2.8 % in healthy control individuals (P < 0.001). By contrast, the frequencies of the common H63D mutation did not differ, and the allele frequencies of the less frequently observed sequence deviations as substitution S65C in the HFE gene and mutation Y250X in the TFR2 gene underlying hemochromatosis type 3 (HFE3) were < 0.02 both in PCT patients and controls. Our results comprise the first molecular studies of both common and rare hemochromatosis gene variants in German PCT patients, indicating a significant role of the C282Y mutation in the pathogenesis of PCT.     

Inheritance of extra triradii of palmar interdigital areas II and IV.

Data obtained from 423 individuals were analyzed for mode of inheritance of extra triradii on palmar interdigital area II and IV separately, and in combination. It indicates that a single dominant allele A for extra triradius in the area II, and an allele D in the area IV, may be responsible for the presence of the patterns in the respective area, with 75 to 80 per cent penetrance. There are numbers of individuals in which extra triradii are present in both interdigital areas II and IV. The mode of inheritance has been estimated from the data obtained and was found to have co-dominant alleles A and D for the presence in their respective areas. Further analysis revealed the existence of three alleles. A and D for presence, and 0 for absence. The alleles A and D are co-dominant, if combined in the genotype AD, but either allele is dominant in heterozygous combination with 0.     

Palmar creases in Spaniards

In a sample of Spanish people (403 males and 513 females) the palmar creases have been studied according to the method of Bali & Chaube (1971). Bimanual differences are not statistically significant, but there is a sexual dimorphism. Comparing the incidence of the open M type defined by Tillner there are no statistical differences as compared with male German series, though they are seen in female series. It is observed that the frequency of the simian crease is in accordance with the variability of European populations.     

Q36R polymorphism of <Emphasis Type="Italic">KiSS</Emphasis>-<Emphasis Type="Italic">1</Emphasis> gene in Brazilian head and neck cancer patients

The KiSS-1 metastasis-suppressor gene (KiSS-1) product (metastin, kisspeptin) is reported to act after binding with the natural ligand of a G-protein coupled receptor and this gene product inhibits chemotaxis, invasion, and metastasis of cells. The aim of this study was to evaluate the Q36R polymorphism of KiSS-1 in patients with head and neck cancer and to compare the results with healthy individuals and its association with clinicopathological parameters. Gender, age, smoking and alcohol consumption were analyzed for 744 individual (252 head and neck cancer patients and in 522 control individuals). The molecular analysis of these individuals was made after extraction of genomic DNA using the SSCP-PCR technique. This study did not reveal any significant differences in genotype frequencies between healthy individuals and patients with head and neck cancer or with the clinical parameters. This study showed an increase frequency of the Q36R polymorphism in pharyngeal cancer.