Definition of Marfan's syndrome in English:

Marfan's syndrome

nounˈmɑːfãzmärˈfäNz

mass nounMedicine

A hereditary disorder of connective tissue, resulting in abnormally long and thin digits and also frequently in optical and cardiovascular defects.
〔医〕马方氏综合征
Example sentencesExamples
- Younger patients with Marfan's syndrome may benefit from surgery in the subacute phase and avoid rupture of a residual saccular aneurysm in the future.
- Most interest has been focused on fibrillin, since it is present in the largest amounts and since mutations in the fibrillin gene are responsible for Marfan's syndrome.
- Orthodontists also play a role in diagnosing systemic conditions that affect facial growth or development of the dentition, such as acromegaly or Marfan's syndrome.
- None had had a previous aortic dissection or had a family history or clinical characteristics of Marfan's syndrome, and in no case was the aortic dissection secondary to chest trauma.
- Causes of dissection include hypertension, Marfan's syndrome, trauma, Ehler's Danlos, coarctation, bicuspid aortic valve and relapsing polychondritis.

Origin

1930s: named after Antonin B. J. Marfan (1858–1942), French paediatrician.

Definition of Marfan's syndrome in US English:

Marfan's syndrome

(also Marfan syndrome)

nounmärˈfäNz

Medicine

A hereditary disorder of connective tissue, resulting in abnormally long and thin digits and also frequently in optical and cardiovascular defects.
〔医〕马方氏综合征
Example sentencesExamples
- Most interest has been focused on fibrillin, since it is present in the largest amounts and since mutations in the fibrillin gene are responsible for Marfan's syndrome.
- Causes of dissection include hypertension, Marfan's syndrome, trauma, Ehler's Danlos, coarctation, bicuspid aortic valve and relapsing polychondritis.
- None had had a previous aortic dissection or had a family history or clinical characteristics of Marfan's syndrome, and in no case was the aortic dissection secondary to chest trauma.
- Younger patients with Marfan's syndrome may benefit from surgery in the subacute phase and avoid rupture of a residual saccular aneurysm in the future.
- Orthodontists also play a role in diagnosing systemic conditions that affect facial growth or development of the dentition, such as acromegaly or Marfan's syndrome.

Origin

1930s: named after Antonin B. J. Marfan (1858–1942), French pediatrician.

词汇	Marfan's syndrome
释义	Definition of Marfan's syndrome in English: Marfan's syndrome nounˈmɑːfãzmärˈfäNz mass nounMedicine A hereditary disorder of connective tissue, resulting in abnormally long and thin digits and also frequently in optical and cardiovascular defects. 〔医〕马方氏综合征 Example sentencesExamples Younger patients with Marfan's syndrome may benefit from surgery in the subacute phase and avoid rupture of a residual saccular aneurysm in the future. Most interest has been focused on fibrillin, since it is present in the largest amounts and since mutations in the fibrillin gene are responsible for Marfan's syndrome. Orthodontists also play a role in diagnosing systemic conditions that affect facial growth or development of the dentition, such as acromegaly or Marfan's syndrome. None had had a previous aortic dissection or had a family history or clinical characteristics of Marfan's syndrome, and in no case was the aortic dissection secondary to chest trauma. Causes of dissection include hypertension, Marfan's syndrome, trauma, Ehler's Danlos, coarctation, bicuspid aortic valve and relapsing polychondritis. Origin 1930s: named after Antonin B. J. Marfan (1858–1942), French paediatrician. Definition of Marfan's syndrome in US English: Marfan's syndrome (also Marfan syndrome) nounmärˈfäNz Medicine A hereditary disorder of connective tissue, resulting in abnormally long and thin digits and also frequently in optical and cardiovascular defects. 〔医〕马方氏综合征 Example sentencesExamples Most interest has been focused on fibrillin, since it is present in the largest amounts and since mutations in the fibrillin gene are responsible for Marfan's syndrome. Causes of dissection include hypertension, Marfan's syndrome, trauma, Ehler's Danlos, coarctation, bicuspid aortic valve and relapsing polychondritis. None had had a previous aortic dissection or had a family history or clinical characteristics of Marfan's syndrome, and in no case was the aortic dissection secondary to chest trauma. Younger patients with Marfan's syndrome may benefit from surgery in the subacute phase and avoid rupture of a residual saccular aneurysm in the future. Orthodontists also play a role in diagnosing systemic conditions that affect facial growth or development of the dentition, such as acromegaly or Marfan's syndrome. Origin 1930s: named after Antonin B. J. Marfan (1858–1942), French pediatrician.
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