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Literature DB >> 3625216

A case of postganglionic cholinergic dysautonomia.

H Takayama, Y Kazahaya, N Kashihara, H Kuroda, S Miyawaki, Z Ota, N Ogawa.

Abstract

A 24 year old female presented with signs and symptoms of postganglionic cholinergic autonomic dysfunction manifested by impaired lachrymation and salivation, mydriasis of the pupil, decreased gastrointestinal motility, atony of the bladder, and sweating and taste disturbance. Clinical and pharmacological studies confirmed that the abnormalities were restricted mainly to the postganglionic cholinergic autonomic systems. The titre of serum complement was low, antinuclear antibodies revealed a diffuse pattern, and anti SS-A antibody was positive, suggesting that this disorder was caused by an immune mechanism.

Entities: Disease Gene

Mesh：

Year: 1987 PMID： 3625216 PMCID： PMC1032133 DOI： 10.1136/jnnp.50.7.915

Source DB: PubMed Journal: J Neurol Neurosurg Psychiatry ISSN： 0022-3050 Impact factor: 10.154

15 in total

A case of postganglionic cholinergic dysautonomia.

Review 1. Subacute dysautonomia with incomplete recovery.

2. Autonomic neuropathy of acute onset.

3. Thrombotic thrombocytopenic purpura complicating Sjögren's syndrome.

4. The neuropathy of Sjögren's syndrome. Trigeminal nerve involvement.

5. Acute pandysautonomia. Clinical and morphologic study.

6. Pure pan-dysautonomia with recovery.

7. Experimental autonomic neuropathy: an immunologically induced disorder of reflex vasomotor function.

8. Acute autonomic neuropathy. Its occurrence in infectious mononucleosis.

9. Two cases of acute pandysautonomia.

10. Acute autonomic neuropathy.

1. Autonomic neuropathy in systemic lupus erythematosus.

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3. Spectral analysis of heart rate and blood pressure variability in primary Sjögren's syndrome.

4. Micturition disturbance in acute idiopathic autonomic neuropathy.

5. Acute autonomic neuropathy with severe gastrointestinal symptoms in children: a case series.