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Two Siblings with Triple-A Syndrome: Endocrinologic and Neurologic Features

Authors :
Nevin Oruc
Banu Sarer Yurekli
Şevki Çetinkalp
Fatma Keklik Karadağ
Mehmet Erdoğan
Nilufer Ozdemir Kutbay
Fusun Saygili
Gokhan Ozgen
Gökçe Kavasoğlu
Ege Üniversitesi
Source :
The Turkish Journal of Endocrinology and Metabolism. 22:45-49
Publication Year :
2018
Publisher :
AVES Publishing Co., 2018.

Abstract

WOS: 000429745000008<br />Triple-A syndrome is a rare, multi-systemic disease and is characterized by adrenal insufficiency, achalasia, or alacrima. The symptoms may also involve neurologic manifestations, including pyramidal findings and peripheral motor neuropathy. Other findings include autonomic dysfunction and cerebellar ataxia. In the present study, we present the case of two siblings with triple-A syndrome with neurologic manifestations. The neurologic abnormalities can lead to misdiagnosis owing to resemblance to the manifestations of other neurologic disorders. Therefore, the cases with triple-A syndrome should be carefully evaluated and examined for clinical and neurophysiologic signs.

Details

ISSN :
13089846 and 13012193
Volume :
22
Database :
OpenAIRE
Journal :
The Turkish Journal of Endocrinology and Metabolism
Accession number :
edsair.doi.dedup.....4183defcd3ac1149b0099ed4395713a1
Full Text :
https://doi.org/10.25179/tjem.2017-56501