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Dermatoglyphics in trisomy 8 mosaicism

✍ Scribed by Blanka Schaumann; Jaroslav Cervenka; Robert J. Gorlin


Book ID
104703955
Publisher
Springer
Year
1974
Tongue
English
Weight
276 KB
Volume
24
Category
Article
ISSN
0340-6717

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Trisomy 8 mosaicism
✍ G. KosztolΓ nyi; E. M. BΓΌhler; P. Elmiger; G. R. Stalder πŸ“‚ Article πŸ“… 1976 πŸ› Springer 🌐 English βš– 907 KB

A 16-year-old boy with trisomy 8 mosaieism is presented. Increased birth weight, delayed psyehomotoric and accelerated somatic development, and mental retardation were noted; he exhibited a prominent forehead, a broad-bridged upturned nose, an everted lower lip, low set dysmorphic ears, strabismus,

Trisomy 8 mosaicism in a with patient te
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## Trisomy 8 Mosaicism in a Patient With Tetraamelia To the Editor: Trisomy 8 is detected in 0.8% of spontaneous abortions . In neoplasias, especially in myeloid leukaemias, trisomy 8 is a frequent somatic aberration . In liveborn infants trisomy 8 almost always is a mosaic condition. The frequen

Trisomy 8 mosaicism in a patient with he
✍ Fowzan S. Alkuraya; David J. Harris πŸ“‚ Article πŸ“… 2005 πŸ› John Wiley and Sons 🌐 English βš– 112 KB πŸ‘ 1 views

Constitutional trisomy 8 mosaicism (CT8M) is a relatively rare trisomy in humans with a characteristic phenotype. We report an infant with the characteristic CT8M phenotype in addition to heterotaxia. A number of chromosomal abnormalities have been reported in association with laterality defects but

Hand dermatoglyphics in trisomy 4p
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A dermatoglyphic analysis of the hands of 16 patients with trisomy for the short arm of chromosome 4 has revealed an increased frequency of whorl patterns on fingertips, presence of axial triradii in position t' on palms and an increase of the main line index. Although of little diagnostic value the

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✍ Margherita Cirillo Silengo; Gianfranco Davi; Giorgio Crua; Piergiorgio Francesch πŸ“‚ Article πŸ“… 1978 πŸ› Springer 🌐 English βš– 186 KB

An 8-year-old male with mental retardation, speech difficulties, and minor congenital anomalies is presented. The clinical findings suggest the trisomy-8 syndrome. The karyotype indicates trisomy-8 mosaicism with trisomic as well as normal cell lines in blood lymphocytes.