Infantile form of muscle phosphofructokinase deficiency in a premature neonate.
Pediatr Int
; 57(4): 746-9, 2015 Aug.
Article
em En
| MEDLINE
| ID: mdl-26108272
ABSTRACT
Muscle phosphofructokinase (PFK) deficiency is a rare autosomal recessive disease. We report the case of a preterm female infant who was diagnosed with the infantile form of phosphofructokinase deficiency due to a lack of PFK activity in her muscles, manifesting at a corrected age of 1 month as floppy infant syndrome, congenital joint contracture, cleft palate and duplication of the pelvicalyceal system. She died at a corrected age of 6 months due to respiratory failure. We further reviewed other infantile cases in the literature. Congenital hypotonia (78.6%), arthrogryposis (64.3%) and other systemic involvement including encephalopathy (35.7%) and cardiomyopathy (21.4%) are common presentations of the infantile form of PFK deficiency. The overall survival rate of the infantile form is low. The early recognition of multiple system involvement is essential to provide better clinical care for infants with the infantile form of PFK deficiency.
Palavras-chave
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Recém-Nascido Prematuro
/
Doença de Depósito de Glicogênio Tipo VII
Tipo de estudo:
Diagnostic_studies
Limite:
Female
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Humans
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Infant
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Newborn
Idioma:
En
Ano de publicação:
2015
Tipo de documento:
Article