FAMILIAL AUTONOMIC DYSFUNCTION
- 23 August 1952
- journal article
- research article
- Published by American Medical Association (AMA) in JAMA
- Vol. 149 (17) , 1532-1535
- https://doi.org/10.1001/jama.1952.02930340016006
Abstract
Up to 1949 there had appeared several isolated case reports1 of what now seem to be examples of a definite clinical entity. This is characterized by evidences of vegetative dysfunction, such as excessive perspiration, drooling, erythematous blotching of the skin, intermittent hypertension, and defective lacrimation; hyporeflexia and emotional instability are also present. In 1949 my co-workers and I reported five illustrative cases.2 Since then our experience with the condition has grown with new cases and repeated observations on old cases. Other hospitals and physicians have made available the records of additional cases, so that we are now able to present a more definitive picture of the condition, based on a total of 33 cases. Their sources are shown in table 1. CLINICAL FEATURES In table 2 the common features are listed and their frequency in this series shown. These are arranged in two groups, the first (group A)Keywords
This publication has 2 references indexed in Scilit:
- HYPOTHALAMIC ATTACKS WITH THALAMIC LESIONArchives of Neurology & Psychiatry, 1945
- THE EFFECT OF SLEEP ON SKIN TEMPERATURE REACTIONS IN A CASE OF ACROCYANOSISJournal of Clinical Investigation, 1939