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Case Report
Hepatic glycogenosis in type 1 diabetes mellitus mimicking Mauriac syndrome
In Ah Jung, Won Kyoung Cho, Yeon Jin Jeon, Shin Hee Kim, Kyoung Soon Cho, So Hyun Park, Min Ho Jung, Byung-Kyu Suh
Clin Exp Pediatr. 2015;58(6):234-237.   Published online June 22, 2015

Hepatic glycogenosis in type 1 diabetes mellitus (DM) can be caused by poor glycemic control due to insulin deficiency, excessive insulin treatment for diabetic ketoacidosis, or excessive glucose administration to control hypoglycemia. Mauriac syndrome, which is characterized by hepatomegaly due to hepatic glycogenosis, growth retardation, delayed puberty, and Cushingoid features, is a rare diabetic complication. We report a case of...

A case of simultaneously identified glycogen storage disease and mucopolysaccharidosis
Ju Young Lee, Jeong Ok Shim, Hye Ran Yang, Ju Young Chang, Choong Ho Shin, Jae Sung Ko, Jeong Kee Seo, Woo Sun Kim, Gyeong Hoon Kang, Jeong Han Song, Jong Won Kim
Clin Exp Pediatr. 2008;51(6):650-654.   Published online June 15, 2008
Glycogen storage disease (GSD) and mucopolysaccharidosis (MPS) are both independently inherited disorders. GSD is a member of a group of genetic disorders involving enzymes responsible for the synthesis and degradation of glycogen. GSD leads to abnormal tissue concentrations of glycogen, primarily in the liver, muscle, or both. MPS is a member of a group of inherited lysosomal storage diseases, which...
A Case of Glycogenosis I.
Se Yoon Eun, Sung Hwan Kim, Sang Il Rhee, Sang Woo Kim, Hye Je Cho, In Ki Park
Clin Exp Pediatr. 1984;27(4):401-406.   Published online April 30, 1984
We experienced a case of Glycogenosis I in eleven-year-old boy. Clinical features were growth retardation, general weakness, abdominal distension due to hepatomegaly. His bone age was retarded, and huge hepatomegaly and both renal hypertropy was seen in CAT. Latoratory findings revealed epinephrine resistant hypoglycemia, hyperuricemia, metabolic acidosis with increased anion gap and acetonuria without glycosuria. Light microscopic findings of liver and...
Original Article
A Clinical Study on Anaphylactoid Purpura.
T K Yoon, T H Lee, S M Shin, S J Lee
Clin Exp Pediatr. 1981;24(12):1185-1192.   Published online December 15, 1981
Anaphylactoid purpura is a common disease in childhood and manifests variable clinical features including hepatomegaly. We analyzed 35 children who were admitted and diagnosed as anaphylactoid purpura at Soon Chun Hyang hospital during the periods of 5 years from September, 1975 to August 1980. The results were as follows: 1)It more frequently affected male than female, in the ratio...
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