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单词 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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更新时间:2025/7/18 4:23:12