TERMIUM Plus®
The Government of Canada’s terminology and linguistic data bank.
DELETION PARTIELLE [4 records]
Record 1 - internal organization data 2023-04-25
Record 1, English
Record 1, Subject field(s)
- Human Diseases - Various
- Genetics
Record 1, Main entry term, English
- monosomy 21
1, record 1, English, monosomy%2021
correct
Record 1, Abbreviations, English
Record 1, Synonyms, English
- monosomy 21 syndrome 2, record 1, English, monosomy%2021%20syndrome
correct
- 21q- deletion syndrome 3, record 1, English, 21q%2D%20deletion%20syndrome
correct
- 21q- syndrome 4, record 1, English, 21q%2D%20syndrome
- antimongolism 5, record 1, English, antimongolism
obsolete, pejorative
Record 1, Textual support, English
Record number: 1, Textual support number: 1 CONT
Monosomy 21 is a chromosomal anomaly characterized by the loss of variable portions of a segment of the long arm of chromosome 21 that leads to an increased risk of birth defects, developmental delay and intellectual deficit. 4, record 1, English, - monosomy%2021
Record 1, Key term(s)
- 21q deletion syndrome
- 21q syndrome
- anti-mongolism
Record 1, French
Record 1, Domaine(s)
- Maladies humaines diverses
- Génétique
Record 1, Main entry term, French
- monosomie 21
1, record 1, French, monosomie%2021
correct, feminine noun
Record 1, Abbreviations, French
Record 1, Synonyms, French
- syndrome de délétion 21q 2, record 1, French, syndrome%20de%20d%C3%A9l%C3%A9tion%2021q
correct, masculine noun
- syndrome 21q 2, record 1, French, syndrome%2021q
masculine noun
Record 1, Textual support, French
Record number: 1, Textual support number: 1 CONT
La monosomie 21 est une anomalie chromosomique caractérisée par une délétion partielle variable d’un segment du bras long du chromosome 21, qui mène à un risque accru de malformations congénitales, de retard de développement et de déficit intellectuel. 2, record 1, French, - monosomie%2021
Record 1, Key term(s)
- syndrome de délétion 21q-
- syndrome 21q-
Record 1, Spanish
Record 1, Campo(s) temático(s)
- Enfermedades humanas varias
- Genética
Record 1, Main entry term, Spanish
- síndrome de monosomía 21
1, record 1, Spanish, s%C3%ADndrome%20de%20monosom%C3%ADa%2021
correct, masculine noun
Record 1, Abbreviations, Spanish
Record 1, Synonyms, Spanish
- síndrome de monosomía del cromosoma 21 1, record 1, Spanish, s%C3%ADndrome%20de%20monosom%C3%ADa%20del%20cromosoma%2021
correct, masculine noun
- monosomía del cromosoma 21 2, record 1, Spanish, monosom%C3%ADa%20del%20cromosoma%2021
correct, feminine noun
- monosomía 21 3, record 1, Spanish, monosom%C3%ADa%2021
correct, feminine noun
Record 1, Textual support, Spanish
Record number: 1, Textual support number: 1 CONT
El síndrome de monosomía del cromosoma 21 se diagnostica por la demostración de una deleción completa o parcial del cromosoma 21, es muy rara y la mayoría de los reportes involucran diferentes translocaciones, mosaicos, deleción parcial del brazo largo o anillos. Existe una marcada variabilidad clínica por lo cual se puede dificultar el diagnóstico. 1, record 1, Spanish, - s%C3%ADndrome%20de%20monosom%C3%ADa%2021
Record 2 - internal organization data 2017-04-27
Record 2, English
Record 2, Subject field(s)
- Musculoskeletal System
Record 2, Main entry term, English
- trigonocephaly 1, record 2, English, trigonocephaly
Record 2, Abbreviations, English
Record 2, Synonyms, English
- trigocephaly 1, record 2, English, trigocephaly
- trigonocephalia 1, record 2, English, trigonocephalia
Record 2, Textual support, English
Record number: 2, Textual support number: 1 DEF
Triangular or egg-shaped head, due to early synostosis of the metopic suture. 1, record 2, English, - trigonocephaly
Record number: 2, Textual support number: 1 CONT
(A new deletion syndrome) Both patients have trigonocephaly with prominent forehead; wide flat nasal bridge; anteverted nostrils; long upper lip; short neck; muscle hypertonia and predominance of whorls on the fingers. 1, record 2, English, - trigonocephaly
Record 2, French
Record 2, Domaine(s)
- Appareil locomoteur (Médecine)
Record 2, Main entry term, French
- trigonocéphalie
1, record 2, French, trigonoc%C3%A9phalie
feminine noun
Record 2, Abbreviations, French
Record 2, Synonyms, French
Record 2, Textual support, French
Record number: 2, Textual support number: 1 DEF
Déformation crânienne caractérisée par le développement en pointe de l’os frontal, donnant au crâne un aspect triangulaire; elle est consécutive à la synostose précoce de la suture métopique (frontale). 1, record 2, French, - trigonoc%C3%A9phalie
Record number: 2, Textual support number: 1 CONT
(Délétion partielle du bras court du 9) L'accentuation de la trigonocéphalie avec constitution d’une véritable crête frontale, l'apparition d’impressions digitiformes, les modifications du fond d’œil [...] et des potentiels évoqués visuels imposent alors une craniotomie dont l'effet semble bénéfique sur le comportement de l'enfant. 1, record 2, French, - trigonoc%C3%A9phalie
Record 2, Spanish
Record 2, Textual support, Spanish
Record 3 - internal organization data 1986-08-13
Record 3, English
Record 3, Subject field(s)
- Genetics
Record 3, Main entry term, English
- interstitial deletion
1, record 3, English, interstitial%20deletion
correct
Record 3, Abbreviations, English
Record 3, Synonyms, English
- intercalary deletion 1, record 3, English, intercalary%20deletion
correct
Record 3, Textual support, English
Record number: 3, Textual support number: 1 DEF
Loss of a portion of a chromosome between two breaks. 1, record 3, English, - interstitial%20deletion
Record number: 3, Textual support number: 1 CONT
(Two-break Rearrangements). 46,XX, del (2) (q22 q 31) = an interstitial deletion in chromosome 2 with break points in region 2 band 2 and region 3 band 1, with a deletion of the intervening segment. 1, record 3, English, - interstitial%20deletion
Record 3, French
Record 3, Domaine(s)
- Génétique
Record 3, Main entry term, French
- délétion interstitielle
1, record 3, French, d%C3%A9l%C3%A9tion%20interstitielle
correct, feminine noun
Record 3, Abbreviations, French
Record 3, Synonyms, French
- délétion intercalaire 1, record 3, French, d%C3%A9l%C3%A9tion%20intercalaire
correct, feminine noun
Record 3, Textual support, French
Record number: 3, Textual support number: 1 DEF
Perte d’une partie de chromosome entre deux cassures. 1, record 3, French, - d%C3%A9l%C3%A9tion%20interstitielle
Record number: 3, Textual support number: 1 CONT
(Trisomie partielle 7q). On explique mal cependant la survenue si fréquente d’un remaniement complexe, à savoir la délétion interstitielle d’un segment chromosomique puis sa translocation sur un autre chromosome de manière interstitielle, si on admet la théorie du télomère. 1, record 3, French, - d%C3%A9l%C3%A9tion%20interstitielle
Record 3, Spanish
Record 3, Textual support, Spanish
Record 4 - internal organization data 1986-08-13
Record 4, English
Record 4, Subject field(s)
- Genetics
Record 4, Main entry term, English
- partial deletion
1, record 4, English, partial%20deletion
correct
Record 4, Abbreviations, English
Record 4, Synonyms, English
Record 4, Textual support, English
Record number: 4, Textual support number: 1 DEF
Loss of a small fragment of chromosome. 1, record 4, English, - partial%20deletion
Record number: 4, Textual support number: 1 CONT
A partial deletion is described by the use of either a minus sign following the given chromosome arm or by descriptive terminology; for example, del 4p or 4p- designates a partial monosomy of chromosome 4. 1, record 4, English, - partial%20deletion
Record 4, French
Record 4, Domaine(s)
- Génétique
Record 4, Main entry term, French
- délétion partielle
1, record 4, French, d%C3%A9l%C3%A9tion%20partielle
correct, feminine noun
Record 4, Abbreviations, French
Record 4, Synonyms, French
Record 4, Textual support, French
Record number: 4, Textual support number: 1 DEF
Perte d’un petit fragment de chromosome. 1, record 4, French, - d%C3%A9l%C3%A9tion%20partielle
Record number: 4, Textual support number: 1 CONT
(Chromosome 4). La distinction entre les chromosomes du groupe B s’est faite avant la découverte des méthodes de marquage en appelant arbitrairement chromosome 5 celui dont la délétion partielle est responsable de la maladie du "cri du chat". 1, record 4, French, - d%C3%A9l%C3%A9tion%20partielle
Record 4, Spanish
Record 4, Textual support, Spanish
Copyright notice for the TERMIUM Plus® data bank
© Public Services and Procurement Canada, 2024
TERMIUM Plus®, the Government of Canada's terminology and linguistic data bank
A product of the Translation Bureau
Features
Language Portal of Canada
Access a collection of Canadian resources on all aspects of English and French, including quizzes.
Writing tools
The Language Portal’s writing tools have a new look! Easy to consult, they give you access to a wealth of information that will help you write better in English and French.
Glossaries and vocabularies
Access Translation Bureau glossaries and vocabularies.
- Date Modified: