Literature DB >> 729197

The dermatoglyphic pattern of the trisomy 10p syndrome.

A Rodewald, S Stengel-Rutkowski.   

Abstract

Dermatoglyphic findings are reported for six members of a family in which two patients have partial trisomy for the short arm of chromosome 10(p13 leads to pter) and there are two unaffected carriers of the balanced translocation t(5;10)(p15;p13). The patterns are compared with those of nine other published cases of trisomy 10p. The following dermatoglyphic features appear to be characteristic for the trisomy 10p syndrome: frequent whorls and a high total ridge count on the finger prints and on the palms, C-lines terminating in space 11 (2nd interdigitum), B-lines terminating in space 9(3rd interdigitum), axial triradii t'', high atd angles, abnormal creases on the palms and soles, and general dysplasia of the papillary ridges.

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Year:  1978        PMID: 729197     DOI: 10.1111/j.1399-0004.1978.tb02098.x

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


  2 in total

1.  New chromosomal dysmorphic syndromes. 2. Trisomy 10p.

Authors:  S Stengel-Rutkowski; J D Murken; R Frankenberger; M Riechert; H Spiess; A Rodewald; J Stene
Journal:  Eur J Pediatr       Date:  1977-10-12       Impact factor: 3.183

2.  Single crease on the 5th finger in medical disorders and in normal population.

Authors:  A Rodewald; H Wischerath
Journal:  J Med Genet       Date:  1979-10       Impact factor: 6.318

  2 in total

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