A Patient with Seckel Syndrome Associated with Partial IgA Deficiency and Idiopathic Thrombocytopenic Purpura
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https://doi.org/10.58600/eurjther.1998-9-1-2-1450-archKeywords:
Seckel syndrome, lgA deficiency, idiopathic thrombocytopenic purpuraAbstract
A 5½-year-old girl with Seckel syndrome associated with partial IgA deficiency and idiopathic. thrombocytopenic purpura has been presented. The patient experienced recurrent infections including upper and lower respiratory tract, gastrointestinal and urinary systems. She had also idiopathic thrombocytopenic purpura at the age of five. Patient with Seckel syndrome presenting frequent injections should be evaluated for immunodeficiencies.
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Seckel HPG: Bird-headed dwarfs. llli nois: Springfield CC Thomas, 1960. P:241
Di Blasi, Belvedere M, Pintacuda S, et al: Seckels syndrome: A case report. J Med 24:75, 1993.
Berkel AI, Ersoy F, Sanal O, Yeğin O: Se rum immunoglobulin and complement le vels in healthy Turkish children. Turk J Pediatr 28:89, 1985
Rappen U, Von Brenndorff I: Cardiac symptoms in two patients with Seckel's syndrome. Monatsschr Kinderhailkd 141:584, 1993
Howanietz H, Frich H, Jedlicka-Köhler 1, Steger H: Report on Seckel's syndrome based on a personel observation. Klin Padiatr 201:139, 1989
Butler MG, Hali BD, Maclean RN, Lozzis CB: Do some patients with Seckel synd rome have hematoligical problems and/or chromosome breakage?. Am J Med Genet 27:645, 1987
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