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)
We have described an infant with familial infantile myasthenia gravis, the rarest of the myasthenic syndromes, which occurs in infants of nonmyasthenic mothers.
Recurrent apnea
and respiratory depression with an absence of
ophthalmoplegia
are features of this syndrome, which if untreated can lead to sudden death.
...
PMID:Familial infantile myasthenia gravis: a preventable cause of sudden death. 397 17
