| Literature DB >> 24650581 |
Pin Fee Chong1, Kohei Haraguchi2, Michiko Torio3, Makiko Kirino4, Reina Ogata2, Masaru Matsukura2, Yasunari Sakai3, Yoshito Ishizaki3, Toshiyuki Yamamoto5, Ryutaro Kira2.
Abstract
Pontine tegmental cap dysplasia (PTCD) is a newly described brainstem malformation with distinct neuroimaging findings, characterized by a flattened ventral pons, cerebellar vermal hypoplasia and vaulted pontine tegmentum that forms a "caplike" or "beaklike" bulge projecting into the fourth ventricle. We describe a 3-month-old infant male who presented with typical neuroradiological findings as well as clinical features of PTCD. Notably, he manifested multiple anomalies with left ocular and facial hypoplasia, bilateral sensorineural hearing loss and rib and vertebral anomalies. Oculoauriculovertebral spectrum (OAVS) was thus considered to be an accompanying phenotype of this patient. The unique comorbidity seen in this patient suggests that PTCD and OAVS may partly share a common mechanism in their pathogenesis.Entities:
Keywords: OAVS; Oculoauriculovertebral spectrum; PTCD; Pontine malformation; Pontine tegmental cap dysplasia
Mesh:
Year: 2014 PMID: 24650581 DOI: 10.1016/j.braindev.2014.02.007
Source DB: PubMed Journal: Brain Dev ISSN: 0387-7604 Impact factor: 1.961