Interruption of oculosympathetic pathway.
- Specialty
- Neurology
- Subspecialty
- Neurology / Neuro-ophthalmology
- Sex & age distribution
- Male: affected; Female: affected; Children: yes
- Gene(s) involved
- None recorded
- Alternative names & eponyms
- Bernard–Horner syndrome
Etiology & mechanism
Central, preganglionic or postganglionic lesion.
Gene(s) involved (0)
No gene recorded for this syndrome.
Symptoms & signs (3)
In plain terms, someone with Horner syndrome may experience the following — click any to explore related syndromes:
Same gene(s)
Other syndromes that involve one of this syndrome's genes.
Overlapping symptoms
Other syndromes that share symptoms with this one.
Drag nodes, scroll to zoom, click a node to open that syndrome.
Shares symptoms with
2 shared
Raeder syndrome
miosis, ptosis
1 shared
Blepharophimosis–ptosis–epicanthus inversus syndrome
ptosis
1 shared
Char syndrome
ptosis
1 shared
Congenital myasthenic syndrome
ptosis
1 shared
Congenital myasthenic syndrome, acetylcholine receptor deficiency
ptosis
1 shared
Congenital myasthenic syndrome, slow-channel type
ptosis
1 shared
Lymphedema–distichiasis syndrome
ptosis
1 shared
Miller Fisher syndrome
ptosis
1 shared
Noonan syndrome
ptosis
1 shared
Orbital apex syndrome
ptosis
Shares genes with
None.
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