Hyperinsulinism in syndromal disorders

被引:22
作者
Meissner, T
Rabl, W
Mohnike, K
Scholl, S
Santer, R
Mayatepek, E
机构
[1] Univ Childrens Hosp, Div Metab & Endocrine Dis, DE-9120 Heidelberg, Germany
[2] Tech Univ, Childrens Hosp, Munich, Germany
[3] Univ Childrens Hosp, Magdeburg, Germany
[4] Univ Childrens Hosp, Hannover, Germany
[5] Univ Childrens Hosp, Kiel, Germany
关键词
congenital central hypoventilation syndrome; congenital disorder of glycosylation; hyperinsulinism; hypoglycaemia; syndromal phenotype;
D O I
10.1080/08035250152509546
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Analysis of a German database comprising a total of 54 patients with neonatal manifestations of persistent hyperinsulinism revealed 5 patients in whom hyperinsulinism was associated with additional clinical symptoms, suggesting an underlying syndromal disorder. Three of the patients presented with a similar yet unknown clinical entity characterized by severe psychomotor retardation, chronic pulmonary disease, hypothyroidism and congenital heart defects. A fourth patient was affected by severe congenital central hypoventilation syndrome. The fifth patient presented with Beckwith-Wiedemann syndrome, with unusually severe and persistent hyperinsulinism requiring subtotal pancreatectomy. Conclusion: Our results indicate that, in addition to the well-known biochemical pathways, more complex pathophysiological mechanisms can result in persistent hyperinsulinism that presents clinically with a disease involving multiple organs.
引用
收藏
页码:856 / 859
页数:4
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