Search

Your search keyword '"Boy M"' showing total 7 results
Start Over Author "Boy M" Publication Year Range More than 50 years ago
7 results on '"Boy M"'

3. [Cytogenetic study of 257 mentally deficient patients in psychiatric hospitals].

Author

Bourgeois M, Bénézech M, Tournier-Zerbid N, Constant-Boy M, and Benazet-Rissou J

Subjects
Adult, Chromosome Aberrations, Chromosomes, Human, 13-15, Chromosomes, Human, 19-20, Chromosomes, Human, 6-12 and X, Dermatoglyphics, Down Syndrome genetics, Epilepsy complications, Female, Humans, Karyotyping, Klinefelter Syndrome genetics, Male, Middle Aged, Mosaicism, Personality Disorders complications, Schizophrenia complications, Sex Chromosome Aberrations genetics, Translocation, Genetic, Turner Syndrome genetics, Intellectual Disability genetics
Abstract

Cytogenetic survey of 257 mentally retarded individuals. A cytogenetic inquiry was undertaken among 257 patients with mental retardation of two psychiatric hospitals. 25 patients show chromosomes anomalies (10%). We found: --18 trisomy 21 (Down's syndrome); --3 sexual chromosome anomalies: 47, XYY syndrome; 47, XYY/46, XY mosaïcism; 47, XXY, or Klinefelter syndrom; --1 partial delection of long arm of chromosome number 18 (46, XX, 18 q--); --3 translocations; 45, XX, t (1, 13) (p 36, q 11); 46, XX, t (5 p--, 18 p+) (p 12, p 11); 46, XY, t (9, 19) (q 21, p 18). We also found 9 large Y chromosomes (46, XY q+), 8 cases of variant chromosomes, 1 case with chromosomes associations..., we report a case of masculine Turner phenotype or Noonan syndrom.

Published
1975

Catalog

Books, media, physical & digital resources
See catalog results