A case of Beals Syndrome in a Filipino child
Acta Medica Philippina
; : 263-265, 2017.
Article
em En
| WPRIM
| ID: wpr-997787
Biblioteca responsável:
WPRO
ABSTRACT
@#We report a case of a 12-year-old Filipino female with crumpled ears, arachnodactyly, camptodactyly, and congenital joint contractures, consistent with Beals syndrome. Marfan syndrome is a common differential diagnosis, since both are caused by mutations in two homologous genes, namely FBN1 and FBN2. Both syndromes share similar characteristics hence, it is essential to differentiate the two, since Marfan syndrome may develop fatal complications, not encountered in Beals Syndrome. Management of Beals syndrome is mainly supportive including physiotherapy and ophthalmologic and cardiovascular evaluation.
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Índice:
WPRIM
Assunto principal:
Síndrome de Marfan
Idioma:
En
Revista:
Acta Medica Philippina
Ano de publicação:
2017
Tipo de documento:
Article