Late‐onset ornithine transcarbamylase deficiency: a rare cause of recurrent abnormal behavior in adults-Reference-Cited by-同舟云学术

Late‐onset ornithine transcarbamylase deficiency: a rare cause of recurrent abnormal behavior in adults

Published:2020-01 Issue:1 Volume:7 Page:
ISSN:2052-8817
Container-title:Acute Medicine & Surgery
language:en
Short-container-title:Acute Med Surg

Author:

Hidaka Masaoki¹^ORCID,Higashi Eiji¹,Uwatoko Takeshi¹,Uwatoko Kiku²,Urashima Mayumi³,Takashima Hiroshi²,Watanabe Yoriko⁴⁵,Kitazono Takanari⁶,Sugimori Hiroshi¹

Affiliation:

1. Department of Cerebrovascular Medicine Stroke Center Saga Prefecture Medical Centre Koseikan SagaJapan

2. Department of Neurology Stroke Center Saga Prefecture Medical Centre Koseikan SagaJapan

3. Department of Pediatrics Saga Prefecture Medical Centre Koseikan SagaJapan

4. Research Institute of Medical Mass Spectrometry Kurume University School of Medicine KurumeJapan

5. Department of Pediatrics and Child Health Kurume University School of Medicine KurumeJapan

6. Department of Medicine and Clinical Science Graduate School of Medical Sciences Kyushu University Fukuoka Japan

Publisher

Wiley

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ams2.565

Reference9 articles.

1. Genotype–Phenotype Correlations in Ornithine Transcarbamylase Deficiency: A Mutation Update

3. Recognition and differential diagnosis of psychosis in primary care;Griswold KS;Am. Fam. Physician.,2015

4. Late onset ornithine transcarbamylase deficiency triggered by an acute increase in protein intake: a review of 10 cases reported in the literature;Barkovich E;Case Rep. Genet.,2020

5. The R40H mutation in a late onset type of human ornithine transcarbamylase deficiency in male patients

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