Prolidase Deficiency with Various Clinical Conditions Including Hyper-IgE and Multiple Lung Bulla Formation-Reference-Cited by-同舟云学术

Prolidase Deficiency with Various Clinical Conditions Including Hyper-IgE and Multiple Lung Bulla Formation

Published:2009 Issue:1 Volume:98 Page:150-152
ISSN:0021-5384
Container-title:Nihon Naika Gakkai Zasshi
language:en
Short-container-title:J. Jpn. Soc. Intern. Med

Author:

Fukumura Atsushi¹,Asaka Tomoya¹,Kasakura Hisato¹,Doshita Takashi¹,Chen WunBill¹,Yokoji Hidehiro¹,Tsuchishima Shuji²,Matsushima Akihiro³,Takeda Kiminobu⁴,Takase Shujiro⁵

Affiliation:

1. Departments of Internal Medicine, Nanao National Hospital

2. Departments of Surgery, Nanao National Hospital

3. Departments of Pediatrics, Nanao National Hospital

4. Departments of Dermatology, Kanazawa Medical University

5. Departments of Gastroenterology, Kanazawa Medical University

Publisher

Japanese Society of Internal Medicine

Subject

General Medicine

Link

https://www.jstage.jst.go.jp/article/naika/98/1/98_150/_pdf

Reference9 articles.

1. 1) Hechtman P: Prolidase deficiency. Scriver CR, et al, eds. The Metabolic & Molecular Bases of Inherited Disease, 8th ed. Mc-Graw-Hill, New York, 2001, 1839-1856.

2. 2) Luder AS, et al: Chronic lung disease and cystic fibrosis phenotype in prolidase deficiency: a newly recognized association. J Pediatr 150: 656-658, 2007.

3. 3) Sekiya M, et al: An autopsy case of prolidase deficiency. Virchows Arch A Pathol Anat Histopathol 406: 125-131, 1985.

4. 4) Lopes I, et al: Prolidase deficiency with hyperimmunoglobulin E: a case report. Pediatr Allergy Immunol 13: 140-142, 2002.

5. 5) Wang H, et al: A nonsense mutation of PEPD in four Amish children with prolidase deficiency. Am J Med Genet A 140: 580-585, 2006.

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