Abstract
We report a female premature infant with bronchopulmonary dysplasia and Sandhoff disease. The clue for diagnosis was the fundoscopy examination. We discuss this rare disease with unusual presentation of intrauterine growth retardation, premature delivery, and bronchopulmonary dysplasia.
Article Type
Case Report
First Page
194
Last Page
197
Recommended Citation
Abdul-Wahab, Atiqa; Bessisso, Mohammed S.; and Elsaid, Mahmoud F.
(2002)
"Sandhoff disease (GM2 gangliosidoses) in a premature patient with bronchopulmonary dysplasia,"
Neurosciences: Vol. 7:
Iss.
3, Article 11.
DOI: https://doi.org/10.17712/1658-3183.1157