%0 Journal Article
%T Nosological delineation of congenital ocular motor apraxia type Cogan: an observational study
%A Christoph Kretzschmar
%A Dirk Mundt
%A Eugen Boltshauser
%A Florian von Deimling
%A Gerhard Kurlemann
%A Hans-Martin B¨¹ttel
%A Iciar S¨¢nchez-Albisua
%A Johannes Buckard
%A J¨¹rgen Seeger
%A Knut Brockmann
%A Martin H£¿ussler
%A Michael Lingen
%A Sandra P. Toelle
%A Sarah Wente
%A Silvia Kinder
%A Simone Schr£¿der
%A Susanne H¨¹bschle
%A Wiebke Maroske
%A Wilfried Diener
%J Archive of "Orphanet Journal of Rare Diseases".
%D 2016
%R 10.1186/s13023-016-0486-z
%X The nosological assignment of congenital ocular motor apraxia type Cogan (COMA) is still controversial. While regarded as a distinct entity by some authorities including the Online Mendelian Inheritance in Man catalog of genetic disorders, others consider COMA merely a clinical symptom
%K Congenital ocular motor apraxia
%K Molar tooth sign
%K Joubert syndrome
%U https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4966602/