Abstract |
A term infant with hydrops fetalis presented with hypotonia, massive splenomegaly, renal failure, and severe hyperferritinemia. Multiple organ failure, myoclonus, and opisthotonus ensued and she died at 15 days of age. High rounded forehead, large open fontanel, and a small recessed chin led to initial premortem diagnosis of Zellweger syndrome, but her plasma profile of long chain fatty acid was normal. Her subsequent clinical course and findings of postmortem examinations were consistent with perinatal lethal form of Gaucher's disease (PLGD). The diagnosis was confirmed by deficiency of enzyme beta-glucocerebrosidase in white blood cells and in cultured fibroblasts. In addition to the crossover features of Zellweger phenotype, this infant exhibited a number of unusual features including, severe hyperferritinemia, rapid progression of splenomegaly, and absence of icthyosis.
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Authors | R Sharma, M L Hudak, A A Perszyk, B R Premachandra, H Li, C Monteiro |
Journal | American journal of perinatology
(Am J Perinatol)
Vol. 17
Issue 4
Pg. 201-6
( 2000)
ISSN: 0735-1631 [Print] United States |
PMID | 11041442
(Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
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Topics |
- Fatal Outcome
- Female
- Gaucher Disease
(complications, diagnosis)
- Glucosylceramidase
(blood)
- Hemosiderosis
(complications, diagnosis)
- Humans
- Infant, Newborn
- Multiple Organ Failure
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