A case of bilateral coronoid process hyperplasia in a child with suspected VACTERL-H syndrome-Reference-Cited by-同舟云学术

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A case of bilateral coronoid process hyperplasia in a child with suspected VACTERL-H syndrome

Published:2018-10-20 Issue:10 Volume:64 Page:605-611
ISSN:0021-5163
Container-title:Japanese Journal of Oral and Maxillofacial Surgery
language:en
Short-container-title:Jpn. J. Oral. Maxillofac. Surg.

Author:

TAKEUCHI Hirohito¹,TANAKA Hideo¹,SAWADA Hiromi²,SHIGA Momotoshi³,HASHIMOTO Kenji¹

Affiliation:

1. Department of Oral and Maxillofacial Surgery, Seirei Hamamatsu General Hospital

2. Department of Orthodontics, Seirei Hamamatsu General Hospital

3. Department of Division of Orofacial Functions & Orthodontics, Kyusyu Dental University

Publisher

Japanese Society of Oral and Maxillofacial Surgeons

Subject

Industrial and Manufacturing Engineering,Environmental Engineering

Link

https://www.jstage.jst.go.jp/article/jjoms/64/10/64_605/_pdf

Reference21 articles.

1. 4) Konstantinidis A and Emmerson A : VACTERL-H syndrome. Infant 9: 158-161, 2013.

2. 6) Herman TE and Siegel MJ : VACTERL-H Syndrome. J Perinatol 22: 496-498, 2002.

3. 7) Evans JA, Stranc LC, et al : VACTERL With Hydrocephalus: Further Delineation of the Syndrome (s). Am J Med Genet 34: 177-182, 1989.

4. 8) Froster UG, Wallner SJ, et al : VACTERL With Hydrocephalus and Branchial Arch Defects: prenatal, Clinical, and autopsy findings in two brothers. Am J Med Genet 62: 169-172, 1996.

5. 9) Aliefendioglu D, Bademci G, et al : VACTERL-H associated with central hypothyroidism: a case report. Genet Couns 18: 331-335, 2007.

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