Biaggioni I, Goldstein D S, Atkinson T, Robertson D
Autonomic Dysfunction Center, Vanderbilt University, Nashville, TN 37232.
Neurology. 1990 Feb;40(2):370-3. doi: 10.1212/wnl.40.2.370.
We report a 42-year-old man with dopamine-beta-hydroxylase deficiency, an autonomic disorder characterized by lifelong severe orthostatic hypotension, ptosis, nasal stuffiness, hyperextensible joints, and retrograde ejaculation. There is isolated deficiency of norepinephrine in both central and peripheral neurons, which contain and release dopamine instead. Dopamine-beta-hydroxylase deficiency should be suspected also in infants presenting with delayed eye opening, hypoglycemia, hypothermia, or hypotension. It can be diagnosed definitively by assay of plasma norepinephrine and dopamine.
我们报告了一名42岁的患有多巴胺β羟化酶缺乏症的男性,这是一种自主神经功能障碍,其特征为终生严重直立性低血压、上睑下垂、鼻塞、关节过度伸展和逆行射精。中枢和外周神经元中均存在去甲肾上腺素的单一缺乏,取而代之的是含有并释放多巴胺。对于出现睁眼延迟、低血糖、体温过低或低血压的婴儿,也应怀疑多巴胺β羟化酶缺乏症。通过检测血浆去甲肾上腺素和多巴胺可明确诊断。