- A Case of Simultaneous Correction of Frontoethmoidal Meningoencephalocele and Hypertelorism
-
Kim HK, Park JH, Lee JH, Chung SM
- KMID: 2203180
- J Korean Soc Plast Reconstr Surg.
- 2008 Jan;35(1):95-98.
PURPOSE: A meningoencephalocele is a congenital malformation involving herniation of the meninges and cerebral tissue through a defect in the skull. For the patient with frontoethmoidal meningoencephalocele with hypertelorism, the... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Median Cleft Face Syndrome
-
Suh KH, Jeong DC, Hur JK, Oh CK
- KMID: 2207617
- J Korean Pediatr Soc.
- 2000 Apr;43(4):583-587.
Median cleft face syndrome is diagnosed by two or more of the following anomalies : ocular hypertelorism, cranium bifidum occultum, median cleft nose, median cleft lip and median cleft premaxilla.... -
- CITED
-
- Close
- SHARE
-
- Close
- Experiences in the treatment of orbital hypertelorism secondary to frontoethmoidal meningoencephaloceles and Saethre-Chotzen syndrome
-
Han KH, Park SG, Song JW, Kang JS
- KMID: 1683915
- J Korean Soc Plast Reconstr Surg.
- 1991 Mar;18(2):287-300.
No abstract available. -
- CITED
-
- Close
- SHARE
-
- Close
- Craniometaphyseal Dysplasia
-
Kim SR, Han YS
- KMID: 2167960
- Arch Plast Surg.
- 2013 Mar;40(2):157-159.
- doi: 10.5999/aps.2013.40.2.157
No abstract available. -
- CITED
-
- Close
- SHARE
-
- Close
- Surgical correction of grade III hypertelorism
-
Haq EU, Qayyum MU, Ilahı MI, Janjua SA, Aslam A, Zahra R
- KMID: 2399921
- J Korean Assoc Oral Maxillofac Surg.
- 2017 Dec;43(Suppl 1):S19-S24.
- doi: 10.5125/jkaoms.2017.43.S1.S19
Orbital hypertelorism is an increased distance between the bony orbits and can be caused by frontonasal malformations, craniofacial clefts, frontoethmoidal encephaloceles, glial tumors or dermoid cysts of the root of... -
- CITED
-
- Close
- SHARE
-
- Close
- Frontonasal dysplasia: A case report
-
Lee SI, Lee SJ, Joo HS
- KMID: 2468780
- Arch Craniofac Surg.
- 2019 Dec;20(6):397-400.
- doi: 10.7181/acfs.2019.00570
Frontonasal dysplasia is an uncommon congenital anomaly with diverse clinical phenotypes and highly variable clinical characteristics, including hypertelorism, a broad nasal root, median facial cleft, a missing or underdeveloped nasal... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of LEOPARD Syndrome
-
Lee HJ, Chung HJ, Cho YH, Chung KY
- KMID: 2302588
- Korean J Dermatol.
- 2005 Jul;43(7):949-952.
LEOPARD syndrome is an autosomal dominantly inherited multiple congenital anomaly syndrome with high penetrance and a markedly variable expression. LEOPARD is an acronym of lentigines, electrocardiographic conduction defects, ocular hypertelorism,... -
- CITED
-
- Close
- SHARE
-
- Close
- Median and Paramedian Craniofacial Cleft
-
Baek RM, Kim YK
- KMID: 1942247
- J Korean Soc Plast Reconstr Surg.
- 2000 Mar;27(2):159-164.
Craniofacial clefts are rare, mysterious and variable congenital anomalies. The incidence of craniofacial clefts is at least 1 per 100,000 live births. The cause of craniofacial clefts remains... -
- CITED
-
- Close
- SHARE
-
- Close
- Experience of Single Stage Treatment of Caniosynostosis, Hypertelorism, Exophthalmos Patient
-
Chung CH, Eun SC, Seo DK, Jo WS, Park SH
- KMID: 2203389
- J Korean Soc Plast Reconstr Surg.
- 2006 Mar;33(2):237-240.
The simultaneous correction of the hypertelorism and exophthalmos combined with craniosynostosis is very rarely performed operative procedures in the world. The craniosynostosis is the congenital anomaly that designates premature fusion... -
- CITED
-
- Close
- SHARE
-
- Close
- Case Report of Rib Bone Graft for Correction of Bifid Nose of Median Facial Cleft
-
Baek RM, Lim JH, Im TK, Ko RY, Yun BH
- KMID: 1961930
- J Korean Cleft Palate-Craniofac Assoc.
- 2002 Oct;3(2):133-136.
Craniofacial cleft is a rare congenital anomaly with a wide range of clinical manifestation and severity of deformity. In 1976, Tessier announced classification system on the basis of anatomical observation... -
- CITED
-
- Close
- SHARE
-
- Close
- Larsen's syndrome: A Case Report
-
Park BM, Han CD, Lee YT
- KMID: 2446180
- J Korean Orthop Assoc.
- 1985 Dec;20(6):1202-1206.
- doi: 10.4055/jkoa.1985.20.6.1202
Larsen's syndrome is a very rare deformity, which is characterized by multiple congenital dislocations with a characteristic facial abnormality. The authors experienced a case of typical Larsen's syndrome that had... -
- CITED
-
- Close
- SHARE
-
- Close
- Ocular Findings in Cri Du Chat Syndrome: A Case Report
-
Kim SK, Kim HS, Kim SH
- KMID: 2337749
- J Korean Ophthalmol Soc.
- 2008 Nov;49(11):1867-1870.
PURPOSE: To report the ophthalmologic examination of an infant who has cri du chat syndome with exotropia and facial abnormalities. CASE SUMMARY: A 7 - month - old infant was confirmed... -
- CITED
-
- Close
- SHARE
-
- Close
- Sincipital Encephalocele: Reort of 3 Operative Cases
-
Suh MS, Hong SK, Kim HJ, Han YP
- KMID: 2187561
- J Korean Neurosurg Soc.
- 1987 Sep;16(3):897-904.
An encephalocele is a protrusion of cranial contents beyond the normal confines of the skull, and sincipital variety denotes and encephalocele with an internal cranial defect localized between the frontal... -
- CITED
-
- Close
- SHARE
-
- Close
- LEOPARD Syndrome with PTPN11 Gene Mutation Showing Six Cardinal Symptoms of LEOPARD
-
Kim J, Kim MR, Kim HJ, Lee KA, Lee MG
- KMID: 2156671
- Ann Dermatol.
- 2011 May;23(2):232-235.
- doi: 10.5021/ad.2011.23.2.232
LEOPARD multiple congenital anomaly syndrome inherited in an autosomal dominant manner. LEOPARD is an acronym for Lentigines, Eletrocardiographic conduction defects, Ocular hypertelorism, Pulmonary valve stenosis, Abnormalities of the genitalia, Retardation... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Multiple Lentigines Syndrome
-
Shin DY, Koo DW, Roh JY
- KMID: 2360368
- Ann Dermatol.
- 1997 Jul;9(3):219-223.
- doi: 10.5021/ad.1997.9.3.219
The multiple lentigines syndrome or LEOPARD syndrome is an autosomal dominantly inherited disorder with a variety of abnormalities and a familial occurrence. This syndrome is characterized by the presence of... -
- CITED
-
- Close
- SHARE
-
- Close
- Anesthetic Experience on the Major Craniofaeial Treatment of the Orbitsl Hypertelorism - A case report
-
Kim SJ, Park KS, Chae BK, Park YC, Gil CI, Shin JS
- KMID: 2349798
- Korean J Anesthesiol.
- 1982 Sep;15(3):364-368.
It is a well known fact that the major craniofacial operation is a complicated procedure. In this procedure, the operative period is extremely long and blood loss is large, extremely... -
- CITED
-
- Close
- SHARE
-
- Close
- Roberts Syndrome: A case report
-
Kim MO, Jung HY, Kim CH, Choi HC
- KMID: 2178783
- J Korean Acad Rehabil Med.
- 2002 Jun;26(3):352-354.
Roberts syndrome is a rare genetic disorder characterized by pre- and postnatal growth retardation, symmetrical limb defects and craniofacial anomalies. A report is given on a 5 year old male... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of 13 Ring Chromosome Syndrome
-
Park CJ, Lim BI, Cho HJ, Song KY, Kim KW
- KMID: 2177141
- J Korean Child Neurol Soc.
- 1998 May;5(2):383-387.
We have experienced a case of 13 ring chromosome in a 40-month-old girl who demonstrated psychomotor retardation with delayed speech, growth retardation, hearing loss(left), microcephaly, trigonocephaly with flat occiput, hypertelorism,... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Stickler Syndrome with Large Eyeballs
-
Lee ES, Kim JA, Jung GY, Choi HS, Park SH
- KMID: 1566112
- J Korean Soc Neonatol.
- 1998 Nov;5(2):242-247.
Stickler syndrome is an autosomal dominant disorder of connective tissue with a wide range of expressivity and incomplete penetrance which is called hereditary progressive arthro-ophthalmopathy. Affected neohates may present with... -
- CITED
-
- Close
- SHARE
-
- Close
- A case of LEOPARD syndrome with cor triatriatum
-
Lee SG, Lee SY, Im SH, Yoo KD, Baek SH, Kim CM, Choi GB
- KMID: 1833206
- Korean J Med.
- 2003 Jul;65(1):99-103.
The LEOPARD syndrome is an acronym and serves as a mnemonic for the features of this autosomal dominant syndrome : L - lentigines (multiple), E - electrocardiographic conduction abnormalities, O... -
- CITED
-
- Close
- SHARE
-
- Close
