[Typical and atypical symptoms in a family with congenital ophthalmoplegia].
D002648:Child; D015785:Eye Diseases, Hereditary; D005355:Fibrosis; D006801:Humans; D007223:Infant; D015835:Ocular Motility Disorders; D009801:Oculomotor Muscles; D009886:Ophthalmoplegia; D010243:Paralysis
MUSCLES, OCULOMOTOR/paralysis; PARALYSIS/in infant and child
Typisches und Atypisches in einer Familie mit kongenitaler Ophthalmoplegie.