Septo-Optic Dysplasia [septo-optická dysplazie]
- Terms
-
de Morsierův syndrom
Morsierova dysplazie
septooptická dysplazie
-
De Morsier Syndrome
Septo-Optic Dysplasia with Growth Hormone Deficiency
Septooptic Dysplasia
A condition resulting from congenital malformations involving the brain. The syndrome of septo-optic dysplasia combines hypoplasia or agenesis of the SEPTUM PELLUCIDUM; CORPUS CALLOSUM and the OPTIC NERVE. The extent of the abnormalities can vary. Septo-optic dysplasia is often associated with abnormalities of the HYPOTHALAMUS and other diencephalic structures, and HYPOPITUITARISM.
- DUI
- D025962 MeSH Browser
- CUI
- M0376630
- Previous indexing
- Hypogonadism (1966-1971); Optic Nerve (1972-2001); Septum Pellucidum (1972-2001)
- History note
- 2002
- Public note
- 2002
Allowable subheadings
- BL
- blood
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification
- CO
- complications 2
- DI
- diagnosis 5
- DG
- diagnostic imaging 2
- DH
- diet therapy
- DT
- drug therapy 1
- EC
- economics
- EM
- embryology 1
- EN
- enzymology
- EP
- epidemiology
- EH
- ethnology
- ET
- etiology 3
- GE
- genetics 3
- HI
- history
- IM
- immunology
- ME
- metabolism
- MI
- microbiology
- MO
- mortality
- NU
- nursing
- PS
- parasitology
- PA
- pathology 2
- PP
- physiopathology 3
- PC
- prevention & control
- PX
- psychology
- RT
- radiotherapy
- RH
- rehabilitation
- SU
- surgery
- TH
- therapy 4
- UR
- urine
- VE
- veterinary
- VI
- virology
Absence of septum pellucidum Disease MeSH Browser
Growth Hormone Deficiency With Pituitary Anomalies Disease MeSH Browser
Hypopituitarism and septooptic 'dysplasia' Disease MeSH Browser
Marshall-Smith syndrome Disease MeSH Browser
Optic nerve hypoplasia, familial bilateral Disease MeSH Browser
Pagon Stephan syndrome Disease MeSH Browser