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PMID: 729197 Published · ppublish English Case Reports Journal Article

The dermatoglyphic pattern of the trisomy 10p syndrome.

Clinical genetics ·Vol. 14 ·No. 6 ·1978-12-00 ·Pages 330-7

Rodewald A, Stengel-Rutkowski S

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.

MeSH Terms
Chromosomes, Human, 6-12 and X Dermatoglyphics Female Humans Male Pedigree Translocation, Genetic Trisomy
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Rodewald A
Stengel-Rutkowski S
Article Info
Journal
Clinical genetics
Abbr.
Clin Genet
ISSN
0009-9163
Published
1978-12-00
Pages
330-7
Language
English
Region
Denmark
NLM ID
0253664
Subset
IM
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