Structured Summary
Abstract
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.
MeSH Record
Classification
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MeSH Record
Synonyms
6 entry terms
- De Morsier Syndrome
- Septo-Optic Dysplasia with Growth Hormone Deficiency
- Septooptic Dysplasia
- Dysplasia, Septooptic
- Septo Optic Dysplasia with Growth Hormone Deficiency
- Septooptic Dysplasias
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
History Note
2002
MeSH Record
Previous Indexing
- Hypogonadism (1966-1971)
- Optic Nerve (1972-2001)
- Septum Pellucidum (1972-2001)
MeSH Hierarchy
Tree Numbers
AMA Style
References
- National Library of Medicine. Septo-Optic Dysplasia. Medical Subject Headings (MeSH). 2026. Unique ID D025962. http://id.nlm.nih.gov/mesh/2026/D025962
- Septo-Optic Dysplasia. In: Wikipedia. https://en.wikipedia.org/wiki/Septo-optic_dysplasia
- Septo-Optic Dysplasia. In: Wikidata. https://www.wikidata.org/wiki/Q2756703