Radiology Teaching Files > Case 162346

never visited VON GIERKE'S DISEASE
Contributed by: Faculty and residents Children's Hospital, Radiologist, Children's Health System, Birmingham, Alabama., USA.
Patient: 16 year old male
History: known history of von Gierke's disease

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Findings: Images demonstrate fatty infiltration of the liver, hepatomegaly, and enhancing hepatic adenomas all characteristic of the patient's known diagnosis.
Diagnosis: von Gierke's disease

von Gierke's disease
Glucose-6-phosphatase deficiency, Glycogen storage disease I, glycogen storage syndrome, glycogenosis type I, glucose-6-phosphatase-deficciency, hepatonephromegalia glycogenica, hepatorenal glycogenosis, liver glycogen disease.
Associated persons:
Edgar Otto Conrad von Gierke
Simon van Creveld
Von Gierke’s is relatively common in a group of hereditary glycogen-storage diseases. This progressive disease is an inborn error of glycogen metabolism due to glucose-6-phosphatase (G6P) deficiency, involving chiefly the liver and kidneys. The liver may become huge and contain as much as 15 percent of glycogen.The symptoms are usually present at birth or appear shortly thereafter. A very long list of symptoms and clinical signs includes failure to thrive, convulsions (hypoglycaemic), retarded growth without disproportion; prominent abdomen due to massive hepatomegaly; adiposity with accumulation of fat in the cheeks, buttocks, and subcutaneous tissues; bleeding tendency; epistaxis; occasionally, steatorrhea; lumbar lordosis; adiposity; skin yellowish xanthomas over joints and buttocks. The muscles are flabby and poorly developed. Gout-related signs.Parenchymal rather than reticuloendothelial cells are involved. Deposition in the heart is known as Pompe's syndrome, in the skeletal muscles as McArdle's syndrome. The disorder occurs in only about 1 in 200,000 persons, affecting both sexes. Afflicted individuals who survive into adulthood suffer primarily from hyperuricaemia and hepatoma. The syndrome is transmitted as an autosomal recessive trait. This was the first recessively inherited disorder shown to be due to deficient activity of a specific intracellular enzyme.
von Gierke gave his account of the association of liver enlargement and disturbed glycogen metabolism in 1929. Simon van Creveld gave further details of the same disorder in 1932 and thereafter the condition was awarded syndromic autonomy. The conjoined eponym enjoyed some favour but the single form is now generally accepted. According to some authors, the disease that carries von Gierke’s name is not the one that he described in 1929. They maintain that von Gierke's patient probably had a deficiency of the glycogen debranching enzyme.

Specifically, (as listed on the web site) Frans Huijing, Professor of Biochemistry and Molecular Biology, University of Miami Schoool of Medicine.

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Additional Details:

Case Number: 162346Last Updated: 10-14-2003
Anatomy: Gastrointestinal (GI)   Pathology: Congenital
Modality: CTExam Date: 09-22-2003Access Level: Readable by all users

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