Sialldosis a rare cause nof neonatal hydrops
Oman Medical Journal. 1999; 16 (2): 7-9
in English
| IMEMR
| ID: emr-52097
ABSTRACT
We report a neonate with Sialidosis type II, a rare metabolic disorder, who presented as hydrops fetalis and early cardiomyopathy. The clinical features, diagnosis and management are discussed. We emphasise that a full metabolic work-up should be performed in any neonate with non-immune hydrops. Also the role of echocardiography in such a case is highlighted
Search on Google
Index:
IMEMR (Eastern Mediterranean)
Main subject:
Infant, Newborn
/
Hydrops Fetalis
/
Cardiomyopathies
Type of study:
Case report
Limits:
Female
/
Humans
Language:
English
Journal:
Oman Med. J.
Year:
1999
Similar
MEDLINE
...
LILACS
LIS