- Update of Diagnostic Evaluation of Craniosynostosis with a Focus on Pediatric Systematic Evaluation and Genetic Studies
-
Hwang SK, Park KS, Park SH, Hwang SK
- KMID: 2192089
- J Korean Neurosurg Soc.
- 2016 May;59(3):214-218.
- doi: 10.3340/jkns.2016.59.3.214
Most craniosynostoses are sporadic, but may have an underlying genetic basis. Secondary and syndromic craniosynostosis accompanies various systemic diseases or associated anomalies. Early detection of an associated disease may facilitate... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Scaphocephaly in a Newborn
-
Joo CU
- KMID: 1676170
- J Korean Pediatr Soc.
- 1985 Mar;28(3):297-300.
No abstract available. -
- CITED
-
- Close
- SHARE
-
- Close
- Craniofacial malformation treatment: craniosynostosis and positional plagiocephaly
-
Park DH, Yoon SH
- KMID: 1787251
- J Korean Med Assoc.
- 2012 Sep;55(9):878-886.
- doi: 10.5124/jkma.2012.55.9.878
After the publication of the modern Virchow's suture fusion hypothesis regarding craniosynostosis, various types of linear craniotomy have been developed. However, after the Moss's functional matrix hypothesis became known, extensive... -
- CITED
-
- Close
- SHARE
-
- Close
- Surgical treatment of acrocephaly: a case report
-
Choi IK, Kim SW, Kim JW
- KMID: 2119295
- J Korean Soc Plast Reconstr Surg.
- 1993 Jul;20(4):838-843.
No abstract available. -
- CITED
-
- Close
- SHARE
-
- Close
- Clinical experience of craniosynostosis
-
Park SH, Lee JY, Ahn HC, Han YS
- KMID: 1684115
- J Korean Soc Plast Reconstr Surg.
- 1992 Sep;19(5):791-800.
No abstract available. -
- CITED
-
- Close
- SHARE
-
- Close
- A surgical correction of the isolated craniosynostosis
-
Cho EJ, Park BY, Lee YH, Choi JU
- KMID: 1684112
- J Korean Soc Plast Reconstr Surg.
- 1992 Sep;19(5):761-771.
No abstract available. -
- CITED
-
- Close
- SHARE
-
- Close
- Fibrous Band between Extraocular Muscles in Unilateral Coronal Synostosis
-
Chung SA, Ha SJ
- KMID: 2469291
- Korean J Ophthalmol.
- 2020 Feb;34(1):88-89.
- doi: 10.3341/kjo.2019.0072
No abstract available. -
- CITED
-
- Close
- SHARE
-
- Close
- Baller-Gerold Syndrome in a Premature Infant with a Mutation in the RECQL4 Gene
-
Kim JS
- KMID: 2466646
- Neonatal Med.
- 2019 Nov;26(4):240-245.
- doi: 10.5385/nm.2019.26.4.240
Baller-Gerold syndrome is a rare autosomal recessive disorder characterized by premature fusion of the cranial sutures and malformation of the upper limb extremities at birth. Although the pathogenesis of Baller-Gerold... -
- CITED
-
- Close
- SHARE
-
- Close
- Preface : Invited Issue Editor, Professor Joon-Ki Kang, and the Topic, Craniosynostosis
-
Kim SK, Wang KC
- KMID: 2192080
- J Korean Neurosurg Soc.
- 2016 May;59(3):185-186.
- doi: 10.3340/jkns.2016.59.3.185
No abstract available. -
- CITED
-
- Close
- SHARE
-
- Close
- A family with Townes-Brocks syndrome with congenital hypothyroidism and a novel mutation of the SALL1 gene
-
Choi WI, Kim JH, Yoo HW, Oh SH
- KMID: 1455878
- Korean J Pediatr.
- 2010 Dec;53(12):1018-1021.
- doi: 10.3345/kjp.2010.53.12.1018
Townes-Brocks syndrome (TBS) is a rare autosomal dominant congenital disorder caused by mutations in the SALL1 gene. Its signs and symptoms overlap with other genetic syndromes, including VACTERL association, Pendred... -
- CITED
-
- Close
- SHARE
-
- Close
- Two Cases of Cerebral Salt Wasting Syndrome Developing after Cranial Vault Remodeling in Craniosynostosis Children
-
Lee SJ, Huh EJ, Byeon JH
- KMID: 2157700
- J Korean Med Sci.
- 2004 Aug;19(4):627-630.
- doi: 10.3346/jkms.2004.19.4.627
Hyponatremia has been recognized as an important postoperative metabolic complication after central nervous system (CNS) operations in children. If not appropriately treated, the postoperative hyponatremia can cause several types of... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Central Diabetes Insipidus Associated with Brachycephaly
-
Kang WS, Namgoong M, Yang JS, Lim BK, Kim JS
- KMID: 2335098
- J Korean Pediatr Soc.
- 1994 Feb;37(2):282-287.
Brachycephaly is a kind of craniosynostosis. Because of premature closure of the coronal suture, the skull is shorter in the anteroposterior diameter but is widened with a high vault and... -
- CITED
-
- Close
- SHARE
-
- Close
- Apert Syndrome: A Report of One Case
-
Hwang JK, Lee DS, Lim JK, Song JS
- KMID: 2445950
- J Korean Orthop Assoc.
- 1986 Oct;21(5):939-942.
- doi: 10.4055/jkoa.1986.21.5.939
Apert described acrocephalosyndactly as a clinical entity in 1906. The classic description of this syndrome includes patient with a combination of acrocephaly and syndactyly of either fingers, toes or both.... -
- CITED
-
- Close
- SHARE
-
- Close
- Two Cases of Apert's Syndrome (Acrocephalosyndactyly)
-
Kim BW, Lee JC, Lee BC
- KMID: 1662726
- J Korean Pediatr Soc.
- 1977 Sep;20(9):711-718.
Apert's syndrome is an uncommon, congenital disturbance in the growth of bone and soft tissue affecting principally the head, the hands and the feet. So there is skull malformation, most... -
- CITED
-
- Close
- SHARE
-
- Close
- Treatment of Nonsyndromic Craniosynostosis Using Multi-Split Osteotomy and Rigid Fixation with Absorbable Plates
-
Nam SB, Nam KW, Lee JW, Song KH, Bae YC
- KMID: 2364350
- Arch Craniofac Surg.
- 2016 Dec;17(4):211-217.
- doi: 10.7181/acfs.2016.17.4.211
BACKGROUND: Nonsyndromic craniosynostosis is a relatively common craniofacial anomaly and various techniques were introduced to achieve its operative goals. Authors found that by using smaller bone fragments than that used... -
- CITED
-
- Close
- SHARE
-
- Close
- Apert Syndrome A Case Report and Analysis of the Reported Cases in Korea
-
Park MS, Choi TH
- KMID: 2444617
- J Korean Orthop Assoc.
- 1988 Jun;23(3):904-910.
- doi: 10.4055/jkoa.1988.23.3.904
Apert syndrome, or acrocephalosyndactyly is a complex of associated malformations, which are craniosynostosis and symmetric complex syndactyly of the hands and feet. The syndrome was first described by Apert in... -
- CITED
-
- Close
- SHARE
-
- Close
- Cerebral Salt Wasting Syndrome After Calvarial Remodeling in Craniosynostosis
-
Byeon JH, Yoo G
- KMID: 1781773
- J Korean Med Sci.
- 2005 Oct;20(5):866-869.
- doi: 10.3346/jkms.2005.20.5.866
Hyponatremia and increased urine output after calvarial remodeling have been noted in pediatric patients with craniosynostosis. If not treated properly, patients develop hypoosmotic conditions that can lead to cerebral edema,... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Acrocephalosyndactyly
-
Cho YS, Park SC, Yun SH, Cho JD
- KMID: 1664174
- J Korean Pediatr Soc.
- 1979 Sep;22(9):818-823.
Apert first described acrocephalosyndactyly as a clinical entity in 1906. Since that time, more than 200 cases have been reported in the world literature. Acrocephalosyndactyly is a rare congenital disturbance... -
- CITED
-
- Close
- SHARE
-
- Close
- Volumetric lipoinjection of the fronto-orbital and temporal complex with adipose stem cells for the aesthetic restoration of sequelae of craniosynostosis
-
Castro-Govea Y, Vela-Martinez A, Treviño-Garcia LA
- KMID: 2409456
- Arch Plast Surg.
- 2018 Mar;45(2):128-134.
- doi: 10.5999/aps.2017.00997
BACKGROUND: Non-syndromic craniosynostosis causes craniofacial asymmetry and may persist after cranioplasty. These postoperative asymmetries are primarily depressions. In some cases, patients may be subjected to pranks and harassment by their... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Crouzon's Disease
-
Cha D, Ahn H
- KMID: 2127626
- J Korean Ophthalmol Soc.
- 1991 Aug;32(8):694-697.
Crouzon's disease is a peculiar type of craniosynostosis which is premature closure of the suture, and deformities of craniofacial bone. Such a many deformities are caused by continuing brain growth... -
- CITED
-
- Close
- SHARE
-
- Close
