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[Wolman's disease in an infant].
Monatsschrift Kinderheilkunde : Organ der Deutschen Gesellschaft fur Kinderheilkunde, 1990Wolman's disease is a rare inherited disorder of lipid metabolism in which large amounts of triglycerides and cholesteryl esters accumulate in the visceral organs. The main clinical features of the infantile form of the disease are failure to thrive, vomiting and diarrhoea, hepatosplenomegaly and radiological evidence of calcification of the adrenals ...
W, Storm +3 more
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Verhandlungen der Deutschen Gesellschaft fur Pathologie, 1979
D B, von Bassewitz +3 more
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D B, von Bassewitz +3 more
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[Wolman's disease (Wolman's syndrome)].
Die Medizinische Welt, 1980W, Permanetter +3 more
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Successful treatment of Wolman disease by unrelated umbilical cord blood transplantation
European Journal of Pediatrics, 2006Jerry Stein, Marsha Zeigler
exaly
Wolman disease successfully treated by bone marrow transplantation
Bone Marrow Transplantation, 2000John E Wagner, Je Wagner, Nk Ramsay
exaly
Prenatal sonographic findings in a case of Wolman's disease
Journal of Clinical Ultrasound, 2018Matthew J Blitz, Nidhi Vohra
exaly
Acta paediatrica Hungarica, 1985
In newborn twins at three hours of age adrenal calcification has been detected. In addition to hepatomegaly, vomiting and diarrhoea, characteristic radiological findings confirmed the diagnosis of the rare heritable lipidosis, Wolman's disease.
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In newborn twins at three hours of age adrenal calcification has been detected. In addition to hepatomegaly, vomiting and diarrhoea, characteristic radiological findings confirmed the diagnosis of the rare heritable lipidosis, Wolman's disease.
openaire +1 more source