- Cranioplasty Using a Modified Split Calvarial Graft Technique in Cleidocranial Dysplasia
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Jung YT, Cho JI, Lee SP
- KMID: 2067110
- J Korean Neurosurg Soc.
- 2015 Jul;58(1):79-82.
- doi: 10.3340/jkns.2015.58.1.79
Cleidocranial dysplasia is a well-documented rare autosomal dominant skeletal dysplasia characterized by hypoplastic/aplastic clavicles, brachycephalic skull, patent sutures and fontanelles, midface hypoplasia, and abnormalities of dentition. Patients with cleidocranial dysplasia... -
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- Cleidocranial Dysostosis: One Case Report
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Yang JH, Jin GG, Seo H
- KMID: 2444548
- J Korean Orthop Assoc.
- 1988 Oct;23(5):1409-1412.
- doi: 10.4055/jkoa.1988.23.5.1409
The cleidocranial dysostosis is characterized by deficient formation of the clavicle, delayed and imperfect ossification of the cranium and less often involvement of other bones. The cleidocranial dysostosis is relatively... -
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- Cleidocranial dysplasia: a preliminary report
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Kim IK, Ha SY, Lee SJ
- KMID: 1690129
- J Korean Assoc Maxillofac Plast Reconstr Surg.
- 1991 Mar;13(1):69-76.
No abstract available. -
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- Cleidocranial Dysostosis One Case Report
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Kim HS, Hong KD, Ha SS, Huh BJ
- KMID: 2445505
- J Korean Orthop Assoc.
- 1990 Apr;25(2):614-618.
- doi: 10.4055/jkoa.1990.25.2.614
Cleidocranial dysostosis is a rare herditary disorder affecting bones that develop by intramembranous formation. The classical features include exaggerated development of the transverse diameter of the skull, delay in the... -
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- Cleidocranial dysostosis occurred in the mother and her son: Case Report
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Park SM, Ahn JS, Lee BS, Lee CW
- KMID: 2423467
- J Korean Orthop Assoc.
- 1994 Oct;29(5):1493-1499.
- doi: 10.4055/jkoa.1994.29.5.1493
Cleidocranial dysostosis is a rare congenital developmental disorder in which membranous bones fail to ossify sufficiently, particularily in the calvarium and the clavicles where fibrous tissue replaces the bone. Authors... -
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- A case study of cleidocranial dysostosis
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Lee JS
- KMID: 2346100
- J Korean Radiol Soc.
- 1966 Nov;2(1):69-70.
- doi: 10.3348/jkrs.1966.2.1.69
No abstract available. -
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- A case of Cleidocranial dysostosis
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Lee YS, Oh KS, kim SH, Kee BK
- KMID: 1676329
- J Korean Pediatr Soc.
- 1985 Sep;28(9):936-939.
No abstract available. -
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- Manifestation and treatment in a cleidocranial dysplasia patient with a RUNX2 (T420I) mutation
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Lee C, Jung HS, Baek JA, Leem DH, Ko SO
- KMID: 2381867
- Maxillofac Plast Reconstr Surg.
- 2015 Nov;37(11):41.
- doi: 10.1186/s40902-015-0042-0
Cleidocranial dysplasia is an autosomal dominant heritable skeletal disorder. The characteristic features of cleidocranial dysplasia (CCD) may include hypoplasia of the clavicle, delayed closure of frontanelles, late tooth eruption, and... -
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- Cleidocranial Dysplasia: Report of a Case
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Jeong SJ, Hong SK
- KMID: 1924094
- Korean J Oral Maxillofac Radiol.
- 2000 Sep;30(3):229-234.
Cleidocranial dysplasia(previously known as cleidocranial dysostosis) is a well-known, rare and hereditary skeletal disorder characterized by a variety of dental abnormalities and as its name implies, striking involvement of the... -
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- Cleidocranial dysostosis: a case report
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Ha SH, Lee SH, Pyo YB, Rim GS
- KMID: 1689932
- J Korean Orthop Assoc.
- 1992 Aug;27(4):1203-1207.
No abstract available. -
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- A Case of Cleidocranial Dysostosis with Leukemia
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eun BL, Han SH, Hong YS, Kim SK
- KMID: 1682625
- J Korean Pediatr Soc.
- 1988 Jul;31(7):930-934.
No abstract available. -
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- Cleidocranial dysplasia: a case report
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Han JW
- KMID: 1573819
- Korean J Oral Maxillofac Radiol.
- 2005 Dec;35(4):225-229.
Cleidocranial dysplasia is a rare, autosomal dominant congenital disorder. A 12-year old female visited with chief complaint of unerupted permanent teeth. Also her father showed severe class III malocclusion. The... -
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- Cleidocranial dysplasia: a case report
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Kim JD, Lee CY, You CH
- KMID: 2270872
- Korean J Oral Maxillofac Radiol.
- 2004 Mar;34(1):55-59.
Cleidocranial dysplasia is a rare and autosomal dominent disorder characterized by aplasia or hypoplasia of the clavicles, an open fontanelle, dental abnormalities, and short stature. A 17-year-old female who presented... -
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- Two Cases Report of Cleidocranial Dysostosis
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Kim KH, Choi IY, Kim SJ, Park SB
- KMID: 2450803
- J Korean Orthop Assoc.
- 1981 Jun;16(2):497-502.
- doi: 10.4055/jkoa.1981.16.2.497
The cleidocranial dysostosis is relatively rare congenital and familial disorder with autosomal dominant inheritance. After the first report of a case of this was that of Cutter in 1870, which... -
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- Aesthetic Facial Correction of Cleidocranial Dysplasia
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Hwang SM, Park B, Hwang MK, Kim MW, Lee JS
- KMID: 2308841
- Arch Craniofac Surg.
- 2016 Jun;17(2):82-85.
- doi: 10.7181/acfs.2016.17.2.82
We report two cases of cleidocranial dysplasia, which was managed without significant craniofacial osteotomy. A mother and daughter, both of normal intelligence, presented with central forehead depression, mid-face hypoplasia, and... -
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- Treatment of a patient with cleidocranial dysplasia using implant-supported bar overdenture: a case report
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Jang JH, Song MS, Kim HM, Kim NH, Eom MY, Koo HM, Yi JK, Jeong JC, Kim SW
- KMID: 1960547
- J Korean Assoc Maxillofac Plast Reconstr Surg.
- 2006 Jan;28(1):80-86.
Cleidocranial dysplasia is rare inherited skeletal dysplasia. It was first reported by Martin in 1765. Subsequently, Marie and Sainton independently documented the criteria of the disease. Cleidocranial dysplasia is a... -
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- Oral Manifestation and Treatment in Cleidocranial Dysplasia Patient: A Case Report
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Jo HW, Choi SY, Kim JW, Byeon KJ, Kim CS
- KMID: 1474302
- J Korean Assoc Maxillofac Plast Reconstr Surg.
- 2009 Sep;31(5):440-443.
Cleidocranial dysplasia(CCD) is a rare syndrome usually caused by an autosomal dominant gene or no apparent genetic cause. The skull is large and short with marked bossing of the frontal... -
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- Case series of cleidocranial dysplasia: Radiographic follow-up study of delayed eruption of impacted permanent teeth
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Yeom HG, Park WJ, Choi EJ, Kang KH, Lee BD
- KMID: 2466554
- Imaging Sci Dent.
- 2019 Dec;49(4):307-315.
- doi: 10.5624/isd.2019.49.4.307
This report describes 3 cases of cleidocranial dysplasia (CCD) and presents relevant findings on long-term follow-up radiographic images of impacted permanent teeth with delayed eruption. Radiographic images of 3 CCD... -
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- A Novel RUNX2 Mutation in a Korean Family with Cleidocranial Dysplasia
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Lee JW, Song J, Shin TJ, Hyun HK, Kim YJ, Lee SH, Kim J, Kim JW
- KMID: 2467077
- J Korean Acad Pediatr Dent.
- 2019 Nov;46(4):409-415.
- doi: 10.5933/JKAPD.2019.46.4.409
Cleidocranial dysplasia (CCD) is an autosomal-dominant disease characterized by the delayed closure of cranial sutures, defects in clavicle formation, supernumerary teeth, and delayed tooth eruption. Defects in the Runt-related transcription... -
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- Complex dental anomalies in a belatedly diagnosed cleidocranial dysplasia patient
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Lu H, Zeng B, Yu D, Jing X, Hu B, Zhao W, Wang Y
- KMID: 2045027
- Imaging Sci Dent.
- 2015 Sep;45(3):187-192.
- doi: 10.5624/isd.2015.45.3.187
Cleidocranial dysplasia (CCD) is a rare congenital disorder, typically characterized by persistently open skull sutures, aplastic or hypoplastic clavicles, and supernumerary teeth. Mutations in the gene encoding the runt-related transcription... -
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