TERMIUM Plus®

The Government of Canada’s terminology and linguistic data bank.

KLINEFELTERS SYNDROME [3 records]

Record 1 2011-01-19

English

Subject field(s)
  • Histology
  • The Genitals
DEF

A chromosomal anomaly with chromosome count 47,XXY sex chromosome constitution; buccal and other cells are usually sex chromatin-positive; patients are male in development, but with seminiferous tubule dysgenesis, elevated urinary gonadotropins, variable gynecomastia, eunuchoid habitus; some patients are chromosomal mosaics, with 2 or more cell lines of different chromosome constitution. (STEME)

French

Domaine(s)
  • Histologie
  • Organes génitaux
DEF

Dysgénésie gonadique masculine due à une anomalie gonosomique avec excès de chromosomes X dont la variété caryotypique la plus fréquente est 47,XXY. Le syndrome de Klinefelter qui s'accompagne d'une atrophie testiculaire avec sclérohyalinose des tubes séminifères n'est pas un état intersexuel, les organes génitaux étant masculins.

CONT

Le phénotype XXXY est souvent considéré comme une variante du syndrome de Klinefelter.

Spanish

Campo(s) temático(s)
  • Histología
  • Órganos genitales
DEF

Anomalía cromosómica hereditaria en la que el varón no desarrolla completamente los testículos, tiene mamas muy desarrolladas y carece de determinados caracteres sexuales secundarios.

Save record 1

Record 2 2002-10-10

English

Subject field(s)
  • The Genitals
  • Symptoms (Medicine)
CONT

Some authors... have discovered a correlation between the imrpovement of hypoandrism and the healing of leg ulcers in Klinefelter's syndrome.

French

Domaine(s)
  • Organes génitaux
  • Symptômes (Médecine)
DEF

Déficience des fonctions sexuelles masculines.

Spanish

Save record 2

Record 3 1985-11-01

English

Subject field(s)
  • Genetics
DEF

Having sex chromatin (Barr body in the nuclei of autosomal cells; a characteristic of the normal female. (DORL)

CONT

(Chromosome mutation) Evidence is available from colour vision studies that either maternal or paternal X chromosome can be lost in chromatin-negative Turner's syndrome and that maternal nondisjunction can account for chromatin-positive Klinefelter's syndrome(GENCYT p. 211)

French

Domaine(s)
  • Génétique
DEF

Qui possède de la chromatine sexuelle (corpuscule de Barr) dans les noyaux des cellules autosomiques; caractéristique des femmes normales.

CONT

(Dysgénésies testiculaires) L'autre concerne 4 frères, un trisomique 21, 2 jumeaux de sexe masculin, dont un mort-né, un garçon avec syndrome de Klinefelter chromatine positive (5 cellules XY; 5 cellules XXY).

Spanish

Save record 3

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