Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UMLS:C0029089 (
ophthalmoplegia
)
3,338
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Sneddon's syndrome
is a rare neurodermatologic disorder that is manifested by multiple cerebrovascular accidents and livedo reticularis. The authors describe two siblings from one family with
Sneddon's syndrome
, suggesting autosomal recessive inheritance. The propositus presented with internuclear
ophthalmoplegia
and ophthalmic artery occlusion. These manifestations as well as the autosomal recessive inheritance have not yet been reported in
Sneddon's syndrome
.
...
PMID:Sneddon's syndrome: neuro-ophthalmologic manifestations in a possible autosomal recessive pattern. 978 55
