Partial trisomy 18(q11 leads to qter) in an infant and aborted fetus resulting from a balanced paternal translocation t(13;18)(q32:q11). 1978

A Rosenmann, and M Isacson, and R Cohen, and M Segal, and M M Cohen

Partial trisomy 18 is described in a two month old female with severe mental, motor and growth retardation, associated with multiple congenital anomalies characteristic of complete trisomy 18. Trisomy for almost all of 18q resulted from adjacent I segregation of a paternally inherited translocation t(13; 18)(q32:q11). The balanced translocation was observed in three generations of the family. Partial trisomy 18q identical to that observed in the proband was found in a subsequent miscarriage.

UI MeSH Term Description Entries
D007223 Infant A child between 1 and 23 months of age. Infants
D007621 Karyotyping Mapping of the KARYOTYPE of a cell. Karyotype Analysis Methods,Analysis Method, Karyotype,Analysis Methods, Karyotype,Karyotype Analysis Method,Karyotypings,Method, Karyotype Analysis,Methods, Karyotype Analysis
D008297 Male Males
D010375 Pedigree The record of descent or ancestry, particularly of a particular condition or trait, indicating individual family members, their relationships, and their status with respect to the trait or condition. Family Tree,Genealogical Tree,Genealogic Tree,Genetic Identity,Identity, Genetic,Family Trees,Genealogic Trees,Genealogical Trees,Genetic Identities,Identities, Genetic,Tree, Family,Tree, Genealogic,Tree, Genealogical,Trees, Family,Trees, Genealogic,Trees, Genealogical
D010641 Phenotype The outward appearance of the individual. It is the product of interactions between genes, and between the GENOTYPE and the environment. Phenotypes
D011247 Pregnancy The status during which female mammals carry their developing young (EMBRYOS or FETUSES) in utero before birth, beginning from FERTILIZATION to BIRTH. Gestation,Pregnancies
D002902 Chromosomes, Human, 16-18 The short, submetacentric human chromosomes, called group E in the human chromosome classification. This group consists of chromosome pairs 16, 17, and 18. Chromosomes E,Group E Chromosomes,Chromosome, Group E,Chromosomes, Group E,E Chromosomes, Group,Group E Chromosome
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000015 Abnormalities, Multiple Congenital abnormalities that affect more than one organ or body structure. Multiple Abnormalities

Related Publications

A Rosenmann, and M Isacson, and R Cohen, and M Segal, and M M Cohen
January 1981, Annales de genetique,
A Rosenmann, and M Isacson, and R Cohen, and M Segal, and M M Cohen
October 1981, Human genetics,
A Rosenmann, and M Isacson, and R Cohen, and M Segal, and M M Cohen
December 2011, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics,
A Rosenmann, and M Isacson, and R Cohen, and M Segal, and M M Cohen
March 1979, Jinrui idengaku zasshi. The Japanese journal of human genetics,
A Rosenmann, and M Isacson, and R Cohen, and M Segal, and M M Cohen
September 1997, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie,
A Rosenmann, and M Isacson, and R Cohen, and M Segal, and M M Cohen
May 1984, Clinical genetics,
A Rosenmann, and M Isacson, and R Cohen, and M Segal, and M M Cohen
December 1973, Annales de genetique,
A Rosenmann, and M Isacson, and R Cohen, and M Segal, and M M Cohen
February 1983, American journal of medical genetics,
A Rosenmann, and M Isacson, and R Cohen, and M Segal, and M M Cohen
February 2021, Medicine,
Copied contents to your clipboard!