Haemorrhagic diathesis as a possible early sign of hereditary fructose intolerance

An infant girl three weeks of age with the leading symptom of skin haemorrhages is presented. On further investigation, the signs of severe hepatic damage with hypofibrinogenaemia and prothrombin complex impairment, and renal tubular dysfunction were disclosed. All these pathological symptoms, which...

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Veröffentlicht in:	European journal of pediatrics 1977-12, Vol.127 (1), p.63-65
Hauptverfasser:	Hosková, A, Mrskos, A
Format:	Artikel
Sprache:	eng
Schlagworte:	Afibrinogenemia - etiology Carbohydrate Metabolism, Inborn Errors - complications Female Fructose Intolerance - complications Fructose Intolerance - diagnosis Fructose Intolerance - genetics Hemorrhagic Disorders - etiology Humans Hypoprothrombinemias - etiology Infant, Newborn
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