Literature DB >> 3757292

Dermatoglyphic peculiarities in families with X-linked mental retardation and fragile site Xq27: a collaborative study.

A Rodewald, U Froster-Iskenius, E Käb, U Langenbeck, A Schinzel, A Schmidt, E Schwinger, P Steinbach, H Veenema, R D Wegner.   

Abstract

The dermatoglyphic patterns of fingertips, palms and soles of 75 male patients with X-linked mental retardation and fra-Xq27 and of 28 obligate female heterozygotes were analyzed and compared with the data from 200 male and 200 female control individuals. The results show that there is a strong association between the fra-X-syndrome and dermatoglyphic peculiarities observed in male patients and also in female heterozygotes. The characteristic dermatoglyphic features of the fra-X-syndrome are: increased frequencies of radial loops, whorls and arches on the fingertips, a pronounced transversal course of palmar ridges, lower a-b RC, absence of c-triradii on the palms, abnormal palmar and plantar creases, dysplasia of the papillary ridges and low frequencies of true patterns on the soles. Some of these patterns were found in the female carriers of fra-Xq27 also. The combination of palmar and plantar patterns, expressed by a "log. score-Index", provides a high degree of discrimination between the male patients with fra-X-syndrome and the control group. A preliminary log. score-Index was developed also for the female heterozygotes. A "phantom picture" of the dermatoglyphic stigmata is constructed. We suggest that dermatoglyphic examination of the members of families suspected for fra-Xq27-syndrome can be useful for predicting this state and for diagnosing male hemizygotes and carrier females.

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Year:  1986        PMID: 3757292     DOI: 10.1111/j.1399-0004.1986.tb00563.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  2 in total

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

Authors:  D Z Loesch; R M Huggins
Journal:  Am J Hum Genet       Date:  1992-05       Impact factor: 11.025

2.  Encephalopathy with intracerebral calcification, white matter lesions, growth hormone deficiency, microcephaly, and retinal degeneration: two sibs confirming a probably distinct entity.

Authors:  C G Bönnemann; P Meinecke; H Reich
Journal:  J Med Genet       Date:  1991-10       Impact factor: 6.318

  2 in total

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