1.Is Rhabdomyolysis a Rare Manifestation in Celiac Disease?.
Mukadder Ayse SELIMOGLU ; Handan ALP ; Vildan ERTEKIN
Yonsei Medical Journal 2004;45(4):759-760
No abstract available.
Celiac Disease/*complications/diagnosis
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Child
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Female
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Humans
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Rhabdomyolysis/diagnosis/*etiology
2.An Unusual Combination of Relapsing and Cholestatic Hepatitis A in Childhood.
Vildan ERTEKIN ; Mukadder Ayse SELIMOGLU ; Zerrin ORBAK
Yonsei Medical Journal 2003;44(5):939-942
Clinical variants of hepatitis A include the prolonged, relapsing and cholestatic forms. Here, the first childhood case of hepatitis A, with a combination of the relapsing and cholestatic forms is presented, a 14-year old boy. In the first phase of the illness, while the AST and ALT levels were declined, th total and direct bilirubin and GGT were increased. The patient was thought to have the cholestatic form of hepatitis A. Du to intense pruritus and high bilirunbin levels, ursodeoxycholic acid (UDCA) therapy was started. On the 17th day, the decreased AST and ALT levels began to increase, reaching levels as high as 484 U/L and 862 U/L, respectively. The UDCA treatment was stopped on the 64th day. On the 164th day, all his laboratory parameters were within normal limits, but the anti-HAV IgM was still positive.
Adolescent
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Alanine Transaminase/blood
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Aspartate Aminotransferases/blood
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Cholestasis/classification/drug therapy/*etiology
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Hepatitis A/*complications
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Human
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Male
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Ursodeoxycholic Acid/therapeutic use
3.First Turkish Patient with Floating Harbor Syndrome with Additional Findings: Cryptorchidim and Microcephaly.
Mukadder Ayse SELIMOGLU ; Erol SELIMOGLU ; Vildan ERTEKIN ; Ibrahim CANER ; Zerrin ORBAK
Yonsei Medical Journal 2004;45(2):334-336
We report the first Turkish patient with Floating Harbor Syndrome (FHS). The 12-year old male patient exhibited classical dysmorphic features of FHS, mental retardation, celiac disease and additional undescribed findings: microcephaly and cryptorchidism.
Abnormalities, Multiple/*pathology
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Child
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Cryptorchidism/*pathology
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Human
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Male
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Microcephaly/*pathology
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*Syndrome
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Turkey
4.Rhabdomyolysis in Celiac Disease.
Vildan ERTEKIN ; Mukadder Ayse SELIMOGLU ; Huseyin TAN ; Buket KILICASLAN
Yonsei Medical Journal 2003;44(2):328-330
A 12-year-old female presented with chronic diarrhea, fatigue, failure to thrive, sudden weakness of her upper and lower extremities and inability to walk. On neurological examination, atrophy was found of the lower extremity muscles, coupled with muscle weakness. Hypokalemia and a high creatine kinase (CK) level were detected. Antigliadin IgA, IgG and antiendomysial antibodies were positive. A duodenal biopsy revealed the classical findings of celiac disease. To our knowledge this is the first childhood case of celiac disease presenting with rhabdomyolysis.
Celiac Disease/blood/*complications
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Child
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Creatine Kinase/blood
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Female
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Human
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Rhabdomyolysis/*etiology