Latest advances in the diagnosis and treatment of Marfan syndrome / 中国当代儿科杂志
Chinese Journal of Contemporary Pediatrics
;
(12): 826-831, 2022.
Article
in Chinese
| WPRIM
| ID: wpr-939670
ABSTRACT
Marfan syndrome (MFS) is a multisystem connective tissue disease with autosomal dominant inheritance. It is mainly caused by FBN1 gene mutation and often has different clinical manifestations. Neonatal MFS is especially rare with severe conditions and a poor prognosis. At present, there is still no radical treatment method for MFS, but early identification, early diagnosis, and early treatment can effectively prolong the life span of patients. This article reviews the latest advances in the diagnosis and treatment of MFS.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Fibrillin-1
/
Marfan Syndrome
/
Mutation
Type of study:
Diagnostic study
/
Screening study
Limits:
Humans
/
Infant, Newborn
Language:
Chinese
Journal:
Chinese Journal of Contemporary Pediatrics
Year:
2022
Type:
Article
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