Meckel-Gruber Syndrome: A Case Who Lived for 5 Months.
Pediatr Neurosurg
; 54(4): 277-280, 2019.
Article
em En
| MEDLINE
| ID: mdl-31261150
ABSTRACT
The Meckel-Gruber syndrome is a rare, congenital, and lethal malformation characterized by typical manifestations such as encephalocele, polycystic kidneys, and polydactyly. Herein, we present a case of a patient with the typical triad as well as facial, ocular, liver, and genital abnormalities who lived for almost 5 months.
Palavras-chave
Texto completo:
1
Coleções:
01-internacional
Contexto em Saúde:
5_ODS3_mortalidade_materna
Base de dados:
MEDLINE
Assunto principal:
Retinose Pigmentar
/
Transtornos da Motilidade Ciliar
/
Polidactilia
/
Encefalocele
/
Doenças Renais Policísticas
Tipo de estudo:
Diagnostic_studies
Limite:
Female
/
Humans
/
Infant
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Male
/
Newborn
/
Pregnancy
Idioma:
En
Revista:
Pediatr Neurosurg
Ano de publicação:
2019
Tipo de documento:
Article