Infantile Marfan syndrome in a Korean tertiary referral center / 소아과
Korean Journal of Pediatrics
;
: 59-64, 2016.
Artículo
en Inglés
| WPRIM
| ID: wpr-110194
ABSTRACT
PURPOSE:
Infantile Marfan syndrome (MFS) is a rare congenital inheritable connective tissue disorder with poor prognosis. This study aimed to evaluate the cardiovascular manifestations and overall prognosis of infantile MFS diagnosed in a tertiary referral center in Korea.METHODS:
Eight patients diagnosed with infantile MFS between 2004 and 2014 were retrospectively evaluated.RESULTS:
Their median age at the time of diagnosis was 2.5 months (range, 0-20 months). The median follow-up period was 25.5 months (range, 0-94 months). The median length at birth was 50.0 cm (range, 48-53 cm); however, height became more prominent over time, and the patients were taller than the 97th percentile at the time of the study. None of the patients had any relevant family history. Four of the 5 patients who underwent DNA sequencing had a fibrillin 1 gene mutation. All the patients with echocardiographic data of the aortic root had a z score of >2. All had mitral and tricuspid valve prolapse, and various degrees of mitral and tricuspid regurgitation. Five patients underwent open-heart surgery, including mitral valve replacement, of whom two required multiple operations. The median age at mitral valve replacement was 28.5 months (range, 5-69 months). Seven patients showed congestive heart failure before surgery or during follow-up, and required multiple anti-heart failure medications. Four patients died of heart failure at a median age of 12 months.CONCLUSION:
The prognosis of infantile MFS is poor; thus, early diagnosis and timely cautious treatment are essential to prevent further morbidity and mortality.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Pronóstico
/
Insuficiencia de la Válvula Tricúspide
/
Ecocardiografía
/
Estudios Retrospectivos
/
Estudios de Seguimiento
/
Mortalidad
/
Prolapso de la Válvula Tricúspide
/
Análisis de Secuencia de ADN
/
Tejido Conectivo
/
Parto
Tipo de estudio:
Estudio diagnóstico
/
Estudio observacional
/
Estudio pronóstico
/
Estudio de tamizaje
Límite:
Humanos
/
Recién Nacido
País/Región como asunto:
Asia
Idioma:
Inglés
Revista:
Korean Journal of Pediatrics
Año:
2016
Tipo del documento:
Artículo
Similares
MEDLINE
...
LILACS
LIS