Fowler-like syndrome with extreme oligohydramnios, growth restriction and without muscular hypoplasia.
Indian Pediatr
;
2003 May; 40(5): 418-23
Artigo
em Inglês
| IMSEAR
| ID: sea-15193
ABSTRACT
We report the seventh family of Fowler like syndrome (proliferative vasculopathy and hydrocephaly-hydrencephaly syndrome) and first case from Indian subcontinent. A 35 weeks extremely growth retarded male baby showed enlarged ventricles, thinned out cerebral cortex, diffuse intra-cerebral as well as peri-ventricular calcification, cerebral and corneal vasculopathy, unilateral micro-ophthalmia along with corneal opacity and depressed pulsatile anterior fontanel. This case was different from others concerning association with extreme oligohydramnios (in contrast to polyhydramnios), extreme growth restriction (in contrast to normal growth) and absence of gross muscle hypoplasia. No causative factors like TORCH infection, chromosomal abnormality or positive family history was noted in this case.
Texto completo:
DisponíveL
Índice:
IMSEAR (Sudeste Asiático)
Assunto principal:
Síndrome
/
Anormalidades Múltiplas
/
Feminino
/
Humanos
/
Masculino
/
Recém-Nascido
/
Gravidez
/
Ventrículos Cerebrais
/
Oligo-Hidrâmnio
/
Evolução Fatal
Idioma:
Inglês
Revista:
Indian Pediatr
Ano de publicação:
2003
Tipo de documento:
Artigo
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