Definition of Noonan syndrome in English:

Noonan syndrome

(also Noonan's syndrome)

noun ˈnuːnən ˌsɪndrəʊm

Medicine

An inherited (autosomal dominant) syndrome typically characterized by short stature, facial dysmorphism, webbed neck, congenital heart disease, and various other abnormalities, resembling Turner's syndrome but without sex chromosome abnormalities.

Origin

1960s. From the name of Jacqueline Anne Noonan (b. 1928), U.S. paediatrician, who first described this syndrome (with D. A. Mehnke) in 1963 (Jrnl. Pediatrics 63 468–70) + syndrome. In β form from the genitive of Noonan + syndrome.

Definition of Noonan syndrome in US English:

Noonan syndrome

(also Noonan's syndrome)

nounˈnuːnən ˌsɪndrəʊm

Medicine

An inherited (autosomal dominant) syndrome typically characterized by short stature, facial dysmorphism, webbed neck, congenital heart disease, and various other abnormalities, resembling Turner's syndrome but without sex chromosome abnormalities.

Origin

1960s. From the name of Jacqueline Anne Noonan (b. 1928), U.S. paediatrician, who first described this syndrome (with D. A. Mehnke) in 1963 ( Jrnl. Pediatrics 63 468–70) + syndrome. In β form from the genitive of Noonan + syndrome.

词汇	Noonan syndrome
释义	Definition of Noonan syndrome in English: Noonan syndrome (also Noonan's syndrome) noun ˈnuːnən ˌsɪndrəʊm Medicine An inherited (autosomal dominant) syndrome typically characterized by short stature, facial dysmorphism, webbed neck, congenital heart disease, and various other abnormalities, resembling Turner's syndrome but without sex chromosome abnormalities. Origin 1960s. From the name of Jacqueline Anne Noonan (b. 1928), U.S. paediatrician, who first described this syndrome (with D. A. Mehnke) in 1963 (Jrnl. Pediatrics 63 468–70) + syndrome. In β form from the genitive of Noonan + syndrome. Definition of Noonan syndrome in US English: Noonan syndrome (also Noonan's syndrome) nounˈnuːnən ˌsɪndrəʊm Medicine An inherited (autosomal dominant) syndrome typically characterized by short stature, facial dysmorphism, webbed neck, congenital heart disease, and various other abnormalities, resembling Turner's syndrome but without sex chromosome abnormalities. Origin 1960s. From the name of Jacqueline Anne Noonan (b. 1928), U.S. paediatrician, who first described this syndrome (with D. A. Mehnke) in 1963 ( Jrnl. Pediatrics 63 468–70) + syndrome. In β form from the genitive of Noonan + syndrome.
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