- A case of septo-optic dysplasia
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Kang SK, Kim SH, Chey MJ, Lee HS
- KMID: 1691572
- J Korean Pediatr Soc.
- 1991 Dec;34(12):1707-1711.
No abstract available. -
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- A Case of Septo-Optic Dysplasia
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Lee WH, Park SH, Shin H
- KMID: 1949694
- J Korean Ophthalmol Soc.
- 1991 Mar;32(3):332-338.
The association of abnormalities of the optic nerves, optic chiasm, and optic tracts with anomalies of the midline structures in the brain-an absent septum pellucidum etc was reported and called... -
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- A Case of Septo-Optic Dysplasia
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On KK, An JW, Myung NH, Kim JD
- KMID: 2107784
- J Korean Ophthalmol Soc.
- 1993 Apr;34(4):366-370.
Septo-optic dysplasia, named by de Morsier in 1956, includes absence of the septum pellucidum, partial or complete agenesis of the corpus callosum, dysplasia of the anterior third ventricle, and bilateral... -
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- A Neonatal Case of Septo-Optic Dysplasia with Schizencephaly
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Lee WH, Kim EY, Park SK
- KMID: 2144511
- J Korean Soc Neonatol.
- 2009 May;16(1):81-84.
Septo-optic dysplasia is a rare congenital disorder characterized by the absence of the septum pallucidum, hypoplasia of the optic chiasma and nerves, and various types of hypothalamic-pituitary dysfunction. Schizencephaly is... -
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- Two Cases of Septo-optic Dysplasia
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Kim JM, Na DR, Park SH, Lee KW, Lee SB, Myung HJ
- KMID: 1662002
- J Korean Neurol Assoc.
- 1986 Dec;4(2):255-259.
Septo-optic dysplasia is an uncommon developmental disorder consisting of septum pellucidum angenesis, optic nerve hypoplasia, congenital nystagmus, seizure and multiple endocrine dysfunction. Clinically mild forms of septo-optic dysplasia and syndrome... -
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- A Case of Septo-Optic Dysplasia in a Neonate
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Rhee HS, Oh YK, Kim HI, Oh JH, Choi SS
- KMID: 2071994
- Korean J Perinatol.
- 1999 Jun;10(2):222-225.
The septo-optic dysplasia, or de Morsier syndrome, is a ventral midline developmental defect of the brain associated with hypoplasia of one or both optic nerves. Agenesis of the septum pellucidum,... -
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- Septo-optic dysplasia
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Kim WJ, Yu YS, Chang BL
- KMID: 1949693
- J Korean Ophthalmol Soc.
- 1991 Mar;32(3):327-330.
Septo-optic dysplasia, first described by de Morsier in 1956, is an uncommon congenital midline structural abnormality of the brain, including agenesis of septum pellucidum, primitive optic ventricle and dysplasia of... -
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- A Case of Septo-Optic Dysplasia
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Lee TK, Kang EJ, Kang ES, Choeh HJ, Choeh K
- KMID: 2104226
- J Korean Pediatr Soc.
- 1996 Feb;39(2):287-290.
Septo-optic dysplasia, as first described by de Morsier, is a rare developmental anomaly involving optic nerve hypolasia, midline anomalies of the brain and variable hypothalamic-pituitary dysfunction. We experienced a case... -
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- A Case of Septo-Optic Dysplasia
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Kim JG, Lee YK, Choi BJ, Lee IG, Whang KT
- KMID: 2177105
- J Korean Child Neurol Soc.
- 1999 May;6(2):400-403.
The septo-optic dysplasia, or de Morsier syndrome is a developmental anomaly characterized by involvement of the septum pellucidum, optic system and hypothalamic-pituitary axis. We had experienced a case of septo-optic... -
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- Septo-optic dysplasia plus diagnosed in a middle-aged woman
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Oh ST, Kang MR, Oh SI, Kim EG, Kim SJ, Seo JH, Chung EJ, Ji KH
- KMID: 2454710
- Ann Clin Neurophysiol.
- 2018 Jul;20(2):85-88.
- doi: 10.14253/acn.2018.20.2.85
Septo-optic dysplasia is a congenital anomaly with diverse phenotypes from normal to mixtures of visual abnormality, endocrine dysfunction, psychomotor retardations and epileptic seizures. It is characterized by optic atrophy, pituitary... -
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- A Case of Septo-Optic Dysplasia
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Cho YS, Jang EY, Cha BH, Lim BK
- KMID: 2177143
- J Korean Child Neurol Soc.
- 1998 May;5(2):393-397.
Septo-optic dysplasia, as first described by de Morsier, is a rare developmental anomaly of absent or hypoplastic septum pellucidum, a primitive optic vesicle, and dysplasia of the optic nerve, chiasm,... -
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- A Case of Septo-Optic Dysplasia-Schizencephaly Complex
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Ahn HS, Ahn BK, Han HJ
- KMID: 2123281
- J Korean Ophthalmol Soc.
- 1993 Jan;34(1):70-74.
Septo-optic dysplasia is diagnosed when optic nerve hypoplasia is combined with dysgenesis of the septum pellucidum and nearly two-thirds of them have hypothalamic-pituitary dysfunction. A number of these patients have... -
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- A Case of Septo-optic Dysplasia Associated with Anterior Pituitary Hormone Abnormalities
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Lee JW, Hwang EK, Kim TH, Yoon HY, Jung JH, Choi YW, Yong SW, Ahn JH, Kim SY, Kim HS, Chung YS
- KMID: 1468493
- J Korean Endocr Soc.
- 2009 Mar;24(1):33-37.
- doi: 10.3803/jkes.2009.24.1.33
Septo-optic dysplasia (SOD) is a rare congenital malformation syndrome that is manifested by a triad of optic nerve hypoplasia, midline brain abnormalities and hypopituitarism. It is known to be associated... -
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- De Morsier`s Syndrome Expressed as Congenital Exotropia
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Han JW, Lee YC
- KMID: 2205501
- J Korean Ophthalmol Soc.
- 1999 Mar;40(3):869-874.
De Morsier syndrome, or septo-optic dysplasia is a developmental anomaly characterized by unilateral or bilaterral optic nerve hypoplasia, agenesis of septum pellucidum, visual disturbance, and a variable spectrum of disturbed... -
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- A Case of Central Diabetes Insipitus Combined with Septo-Optic Dysplasia and Schizencephaly in 31-year-old Woman
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Kim SK, Jung TS, Hahm JR, Lee SM, Moon SW, Lee KJ, Chung SI
- KMID: 1523103
- J Korean Endocr Soc.
- 2007 Oct;22(5):339-343.
- doi: 10.3803/jkes.2007.22.5.339
A 31-year-old woman was referred to our hospital for evaluation and management of poorly controlled epilepsy. The patient had been taking anti-epileptic drugs for six years. An MRI imaging study... -
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- Septooptic Dysplasia: A Case Report
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Kim JH, Choi DS, Lee CW, Kim S, Kim SH, Lee SW, Ha JH, Sakong JK, Lee HK
- KMID: 2334930
- J Korean Radiol Soc.
- 2001 Sep;45(3):251-253.
Septooptic dysplasia is a rare anterior midline anomaly considered to be a mild form of lobar holoprosencephaly. We describe a case with unilateral optic nerve hypoplasia and the absence of... -
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- A Case of Septo-Optic Dysplasia Resulting in Central Diabetes Insipidus and Nonobstructive Bilateral Hydronephrosis
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Kim JH, Lee KB, Lee J, Nam SM, Lee KW, Hwang EG, Gil G
- KMID: 1710033
- Korean J Med.
- 2014 Aug;87(2):209-214.
- doi: 10.3904/kjm.2014.87.2.209
A 27-year-old male with nonobstructive hydronephrosis was referred from the urology department for polyuria evaluation and management. The patient was hospitalized for urinary tract infection and cystostomy was performed due... -
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- Clinical Manifestations of Optic Nerve Hypoplasia
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Kim EA, Hong JS, Chang WH, Kim MM
- KMID: 2110353
- J Korean Ophthalmol Soc.
- 2006 Sep;47(9):1465-1471.
PURPOSE: To estimate the baseline demographic and ocular characteristics of patients with optic nerve hypoplasia (ONH), and to analyze the different features and frequency of coexistent CNS abnormalities and pituitary... -
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- Focal Transmantle Dysplasia: MRI and Clinical Manifestations in 5 Cases
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Kim CH, Choi CG, Lee SA
- KMID: 2186006
- J Korean Neurol Assoc.
- 2001 Nov;19(6):614-618.
BACKGROUND: Recently, focal transmantle dysplasia has been proposed to be a specific malformation of cortical development resulting from abnormal stem cell proliferation. Its clinical and imaging characteristics are not well... -
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- Schizencephaly: An Analysis of Clinical and Neuroradiologic Findings
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Jo KD, Hwang YM, Lee MC
- KMID: 1686773
- J Korean Neurol Assoc.
- 1993 Sep;11(3):404-414.
Schizencephaly is a congenital brain anomaly, a disorder of cell migration characterized by gray matter-lined clefts, which is caused by faulty migration of the subependymal neuroblasts. The cleft may be... -
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