Multiple endocrine neoplasia type 2 and autoimmune polyendocrine syndromes (type 1 diabetes mellitus and Graves’ disease) in a 16-year-old male with Kabuki syndrome-Reference-Cited by-同舟云学术

Multiple endocrine neoplasia type 2 and autoimmune polyendocrine syndromes (type 1 diabetes mellitus and Graves’ disease) in a 16-year-old male with Kabuki syndrome

Published:2022 Issue:10 Volume:69 Page:1211-1216
ISSN:0918-8959
Container-title:Endocrine Journal
language:en
Short-container-title:Endocr J

Author:

Park Esther¹,Kim Min-Sun²,Noh Eu Seon²,Lee Ji-Eun³,Kim Su Jin³,Kwon Young Se³,Cho Sung Yoon²

Affiliation:

1. Department of Pediatrics, Jeonbuk National University Hospital, Jeonju, Korea

2. Department of Pediatrics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea

3. Department of Pediatrics, Inha University Hospital, Inha University College of Medicine, Incheon, Korea

Publisher

Japan Endocrine Society

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

https://www.jstage.jst.go.jp/article/endocrj/69/10/69_EJ22-0084/_pdf

Reference32 articles.

1. 1 Moline J, Eng C (2011) Multiple endocrine neoplasia type 2: an overview. Genet Med 13: 755–764.

2. 2 Lenders JW, Eisenhofer G, Mannelli M, Pacak K (2005) Phaeochromocytoma. Lancet 366: 665–675.

3. 3 Derrou S, Bouziane T, Salhi H, El Ouahabi H (2021) Pheochromocytoma and glucoregulation disorders. Ann Afr Med 20: 42–45.

4. 4 Bholah R, Bunchman TE (2017) Review of pediatric pheochromocytoma and paraganglioma. Front Pediatr 5: 155.

5. 5 Farrugia FA, Charalampopoulos A (2019) Pheochromocytoma. Endocr Regul 53: 191–212.

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