2. Superior oblique tendon sheath
Syndrome
Named by Brown 1950.
It is usually congenital but
occasionally may be acquired.
3. Brown’s syndrome is usually unilateral with
less than 10% of bilateral cases;
There is no preference for the right or left
eye.
Females are affected with the same
frequency as males
There does not appear to be any genetic
basis for the disorder.
Most patients maintain binocular single vision
4. CONGENITAL:
Idiopathic
Congenital click syndrome, where there is
impaired movement of the superior oblique
tendon through the trochlea.
ACQUIRED:
Damage to the trochlea or superior oblique
tendon.
Inflammation of the tendon, which may be
caused by Rheumatoid arthritis, sinusitis, and
scleritis.
CONT’D
CLASSIFICATION
5. Right Brown syndrome will have the following
characteristics
◦ MAJOR SIGNS:
Usually straight in the primary position
Limited right elevation in adduction
Normal right elevation in abduction
No superior oblique over-action
Positive forced duction test on elevating the
globe in adduction
BROWN’S SYNDROME CONT’D
6. ◦VARIABLE SIGNS:
Down-shoot in adduction
Hypo-tropia in primary position
Abnormal head posture with ipsilateral head tilt
and chin elevation
7.
8. CONGENITAL CASES:
Do NOT usually require treatment
Surgery is indicated in cases of
Primary position hypo-tropia
Anomalous head posture
Recommended procedure for
congenital cases is SUPERIOR OBLIQUE
WEAKENING
BROWN’S SYNDROME CONT’D
9. ACQUIRED CASES:
May benefit from STEROIDS, orally or by
injection near the trochlea, together with
TREATMENT OF THE UNDERLYING CAUSE.
10.
11. Inferior oblique palsy
Double elevator palsy (MED)
Orbital blow out fracture
Ocular fibrosis syndrome
12. To understand Brown’s syndrome
You have to understand relationships.
Particularly the relationship between
the superior and inferior oblique.