Hoffmann M H, Vadstrup S
Centralsygehuset i Nykøbing Falster, medicinsk afdeling.
Ugeskr Laeger. 2000 May 8;162(19):2755-6.
A 39 year-old woman was diagnosed with DiGeorge's syndrome based on newly diagnosed hypocalcaemia, appearance and history. The patient had congenital cardiovascular malformations, mild mental retardation and ear malformations, and during infancy and childhood suffered from failure to thrive and frequent infections. In children with conotruncal heart malformation, hypocalcaemia and hypoplasia of the thymus in combination it is estimated that chromosome 22q11 deletion is present in almost 100%. The syndrome is probably underdiagnosed.
一名39岁女性因新诊断的低钙血症、外貌及病史被诊断为迪格奥尔格综合征。该患者有先天性心血管畸形、轻度智力发育迟缓及耳部畸形,在婴儿期和儿童期曾出现生长发育迟缓及频繁感染。在合并圆锥动脉干心脏畸形、低钙血症及胸腺发育不全的儿童中,估计几乎100%存在22q11染色体缺失。该综合征可能存在诊断不足的情况。