MeSH Browser

MeSH Heading: Trochlear Nerve Diseases
Tree Number(s): C10.292.850
Unique ID: D020432
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D020432
Annotation: neopl: coord IM with CRANIAL NERVE NEOPLASMS (IM) + histol type of neopl (IM)
Scope Note: Diseases of the fourth cranial (trochlear) nerve or its nucleus in the midbrain. The nerve crosses as it exits the midbrain dorsally and may be injured along its course through the intracranial space, cavernous sinus, superior orbital fissure, or orbit. Clinical manifestations include weakness of the superior oblique muscle which causes vertical DIPLOPIA that is maximal when the affected eye is adducted and directed inferiorly. Head tilt may be seen as a compensatory mechanism for diplopia and rotation of the visual axis. Common etiologies include CRANIOCEREBRAL TRAUMA and INFRATENTORIAL NEOPLASMS.
Entry Version: TROCHLEAR NERVE DIS
Entry Term(s): Cranial Nerve IV Diseases; Fourth Cranial Nerve Diseases; Fourth Cranial Nerve Palsy; Fourth Nerve Palsy; Neurogenic Superior Oblique Palsy; Superior Oblique Myokymia; Superior Oblique Palsy, Neurogenic; Trochlear Nerve Disorders; Trochlear Nerve Palsy; Trochlear Neuropathy
Previous Indexing: Cranial Nerve Diseases (1981-1999); Trochlear Nerve (1965-1999)
Public MeSH Note: 2000
History Note: 2000
Date Established: 2000/01/01
Date of Entry: 1999/11/03
Revision Date: 2001/07/25

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

congenital (CN)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Concept UI: M0328652
Scope Note: Diseases of the fourth cranial (trochlear) nerve or its nucleus in the midbrain. The nerve crosses as it exits the midbrain dorsally and may be injured along its course through the intracranial space, cavernous sinus, superior orbital fissure, or orbit. Clinical manifestations include weakness of the superior oblique muscle which causes vertical DIPLOPIA that is maximal when the affected eye is adducted and directed inferiorly. Head tilt may be seen as a compensatory mechanism for diplopia and rotation of the visual axis. Common etiologies include CRANIOCEREBRAL TRAUMA and INFRATENTORIAL NEOPLASMS.
Terms: Trochlear Nerve Diseases Preferred Term
Term UI T358652
Date10/12/1999
LexicalTag NON
ThesaurusID NLM (2000); Trochlear Neuropathy
Term UI T370938
Date10/12/1999
LexicalTag NON
ThesaurusID NLM (2000); Trochlear Nerve Disorders
Term UI T370937
Date10/12/1999
LexicalTag NON
ThesaurusID NLM (2000); Cranial Nerve IV Diseases
Term UI T370935
Date10/12/1999
LexicalTag NON
ThesaurusID NLM (2000); Fourth Cranial Nerve Diseases
Term UI T370936
Date10/12/1999
LexicalTag NON
ThesaurusID NLM (2000)

Trochlear Nerve Diseases MeSH Descriptor Data 2024