- Agenesis of Corpus Callosum
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Jun BY, Choi JU
- KMID: 1953116
- J Korean Neurosurg Soc.
- 1988 Dec;17(6):1317-1322.
Thirty three cases with agenesis of the corpus callosum were reviewed from the base of brain CT findings for last 7 years. Clinical features, associated clinical anomalies and CT findings... -
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- Agenesis of corpus callosum-two cases report
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Kweon SY, Seo JW, Kim GH, Chung EC, Koo HS
- KMID: 1945986
- J Korean Pediatr Soc.
- 1992 Jan;35(1):113-121.
No abstract available. -
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- A case of agenesis of corpus callosum
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Kim SM, Bae CH, Park IH, Ro CS, Kim YJ, Lee HJ
- KMID: 1691657
- J Korean Pediatr Soc.
- 1991 Oct;34(10):1433-1438.
No abstract available. -
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- A Case of Corpus Callosum Agenesis with Ileal Atresia and Duplication
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Chun KA, Ham YD, Jeong JH, Lee JH, Kim HS
- KMID: 2207504
- J Korean Pediatr Soc.
- 2000 Aug;43(8):1127-1131.
Agenesis of corpus callosum occurs sporadically and may be transmitted as sex-linked, or autosomal-dominant or recessive traits. It has been associated with different syndromes. Clinical pictures vary from severe intellectual and neurologic... -
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- A Case of Complete Agenesis of Corpus Callosum
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Kim JJ, Shin CS, Yun CS, Kim SM, Kim CS, Bae KH, Park JS, Han KS, Ju JY
- KMID: 2272116
- Korean J Obstet Gynecol.
- 2003 Jul;46(7):1461-1465.
The corpus callosum is the main interhemispheric connection in human brain. Agenesis of corpus callosum may partial or complete, and it may have not functional abnormalities. Its prenatal sonographic diagnosis... -
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- A Case of Acrocallosal Syndrome with Developmental Delay: A case report
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Cho JH, Shin DH, Lee ES, Yoon CH, Shin HS
- KMID: 2323974
- J Korean Acad Rehabil Med.
- 2003 Dec;27(6):997-999.
Agenesis of the corpus callosum is a frequent anomaly that presents with a spectrum of clinical features and exhibits variable findings in neurological studies. Callosal agenesis may be an isolated... -
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- A Case of Agenesis of Corpus Callosum with Chromosome anomaly
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Park JH, Lee GS, Kim SJ, Shim SI, Kim SY, Yoo WJ, Baik EJ, Shin JC, Kim SP
- KMID: 2261805
- Korean J Obstet Gynecol.
- 2000 Jan;43(1):137-140.
The corpus callosum consists of white fibers connecting the cerebral hemispheres. Agenesis of the corpus callosum is an uncommon congenital anomaly which is easily diagnosed in the postnatal period by... -
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- Agenesis of corpus callosum prenatally diagnosed with fetal MRI: case report
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Han JW, Oh MJ, Kim KA, Song SH, Yeo MK, Lee JK, Hur JY, Saw HS, Park YK
- KMID: 2272711
- Korean J Obstet Gynecol.
- 2005 Oct;48(10):2414-2421.
Agenesis of corpus callosum is the cerebral malformations whose prognosis is uncertain. But the complete agenesis shows more poor prognosis than partial agenesis. So, the type of agenesis can affect... -
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- A Case of Potter Syndrome Syndrome Accompanied with Partial Agenesis of Corpus Callosum
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Jang SS, Suh BC, Rhee KH, Moon SJ, Lee KS, Park BT, Hong EK
- KMID: 1677152
- J Korean Pediatr Soc.
- 1987 Nov;30(11):1287-1293.
No abstract available. -
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- Aicardi Syndrome: A case report
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Moon JL, Jung KH, Kang SY
- KMID: 2323451
- J Korean Acad Rehabil Med.
- 2000 Jun;24(3):576-581.
Aicardi syndrome is defined by the clinical triad infantile spasms, agenesis of the corpus callosum, and pathognomonic chorioretinal lacunae. Infantile spasm begins at early infancy and tends to be controlled... -
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- A Case of 4q Deletion with Partial Agenesis of Corpus Callosum
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Kang MN, Lim IS, Kim BE, Chey MJ, Kim SW
- KMID: 2335589
- J Korean Pediatr Soc.
- 2002 Feb;45(2):273-277.
Syndrome of 4q deletion is characterized by an abnormal shape of the skull, craniofacial dysmorphism, cardiovascular malformations, genitourinary defects, limb and digital anomalies, and developmental delay. We experienced a case... -
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- A Case of Diffuse Cerebral Cortical Dysplasia and Partial Agenesis of Corpus Callosum in Seckel Syndrome
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Kim MA, Lee S, Chung HJ
- KMID: 1468164
- J Korean Child Neurol Soc.
- 2009 May;17(1):84-89.
Seckel syndrome is a rare autosomal recessive disorder characterized by low birth weight, short but proportionate stature, microcephaly, moderate to severe mental retardation and typical facial features mimicking bird including... -
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- Prenatally diagnosed agenesis of corpus callosum
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Kim GJ, Lee ES, Lee EJ, Han SS, Lee SH, Kim DH, Lee JJ, Yun SW
- KMID: 2273812
- Korean J Obstet Gynecol.
- 2009 Dec;52(12):1239-1244.
OBJECTIVE: To report the clinical characteristics of the fetuses with agenesis of corpus callosum (ACC) diagnosed by prenatal ultrasonography. METHODS: Between 1998 and 2007, total twenty-two cases of ACC were identified.... -
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- A Case of Aase-Smith Syndrome
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Kim DJ, Seol IJ
- KMID: 1961853
- J Korean Child Neurol Soc.
- 1998 Oct;6(1):113-117.
The Aase-Smith syndrome is characterized by Dandy-walker malformation, hand abnormalities, joint contractures of the hands, and cleft palate. It is known to be inherited as autosomal dominant trait and to... -
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- Clinical outcomes and neurodevelopmental outcome of prenatally diagnosed agenesis of corpus callosum in single center of Korea
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Kim SE, Jang HI, Chang KH, Sung JH, Lee J, Lee J, Choi SJ, Oh SY, Roh CR, Kim JH
- KMID: 2383202
- Obstet Gynecol Sci.
- 2017 Jan;60(1):8-17.
- doi: 10.5468/ogs.2017.60.1.8
OBJECTIVE: With recent advances and frequent use of prenatal ultrasound, the antenatal diagnosis of agenesis of the corpus callosum (ACC) is not rare in obstetrics practices. However, information regarding the... -
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- A Case of Pai Syndrome: First Reported Case in Korea
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Hong M, Nam SW, Lee YK, Ko SY, Shin SM
- KMID: 1917228
- Korean J Perinatol.
- 2014 Mar;25(1):17-21.
- doi: 10.14734/kjp.2014.25.1.17
Pai syndrome is a rare disorder, first described in 1987. Diagnostic criteria are the presence of the nasal polyp and one of the following: midline cleft lip, congenital polyp of... -
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- A Case of Neuronal Heterotopia
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Joo JH, Seok EJ, Kim MJ, Seo SS
- KMID: 2335267
- J Korean Pediatr Soc.
- 1997 Aug;40(8):1173-1177.
Neuronal migrational disorders of the brain represent abnormalities in the formation of the neocortex caused by faulty migration of the subependymal neuroblasts. The neuroblasts normally migrate between the sixth and... -
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- Miller-Dieker Syndrome in an Extremely Low Birth Weight Infant
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Park SJ, Lee NR, Bae MH, Han YM, Byun SY, Park KH
- KMID: 2409125
- Perinatology.
- 2017 Dec;28(4):162-165.
- doi: 10.14734/PN.2017.28.4.162
Miller-Dieker syndrome (MDS) is characterized by severe lissencephaly and facial dysmorphism including the prominent forehead, bitemporal hollowing, a short nose with upturned nares, a protuberant upper lip, and a small... -
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- A Case of Genitopatellar Syndrome
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Kim HJ, Cha JH, Lee SJ, Park EA
- KMID: 1876151
- Korean J Perinatol.
- 2005 Mar;16(1):49-53.
We report a female with genitopatellar syndrome, a recently identified arthrogryposis syndrome. Genitopatellar syndrome is a suggested autosomal recessive disorder, which is characterized by absent patellae, genital and renal anomalies,... -
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- A Case of Greig Cephalopolysyndactyly Syndrome
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Shin SH, Kim JW, Lee YA, Yoon HS, Cho HC
- KMID: 1946284
- J Korean Pediatr Soc.
- 2000 Jan;43(1):128-132.
Greig cephalopolysyndactyly syndrome (GCPS) is a disorder characterized by postaxial polydactyly of the hand, broad or occasionally bifid thumbs, preaxial polydactyly of the feet, broad halluces, syndactyly of the fingers... -
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