A Case of New Dysautonomia-Like Disorder Found in Japan
作者:
T. Suzuki,
S. Higa,
A. Hayashi,
T. Nakagawa,
K. Fujii,
Y. Sato,
T. Oura,
期刊:
European Neurology
(Karger Available online 1976)
卷期:
Volume 14,
issue 2
页码: 146-160
ISSN:0014-3022
年代: 1976
DOI:10.1159/000114737
出版商: S. Karger AG
关键词: Familial dysautonomia;Dysautonomia-like disorder;Catecholamines
数据来源: Karger
摘要:
A case of new dysautonomia-like disorder in a Japanese infant is reported. The patient showed almost all of the essential criteria for the diagnosis of familial dysautonomia. Results of pharmacologic tests and urinary excretion patterns of catecholamines and their metabolites were also compatible with the disorder. But he lacked some important clinical findings, such as lifelong hypolacrimia, skin blotching, excessive sweating and labile blood pressure. Precise observations of clinical features and literatures on non-Jewish cases of familial dysautonomia lent evidence that this case suffered from a new dysautonomia-like disorder.
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