Nosological delineation of congenital ocular motor apraxia type Cogan: an observational study
2016
Background The
nosologicalassignment of congenital ocular motor
apraxiatype Cogan (
COMA) is still controversial. While regarded as a distinct entity by some authorities including the Online
Mendelian Inheritancein Man catalog of
genetic disorders, others consider
COMAmerely a clinical symptom.
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