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A case of pontine tegmental cap dysplasia with comorbidity of oculoauriculovertebral spectrum. | LitMetric

AI Article Synopsis

  • Pontine tegmental cap dysplasia (PTCD) is a newly identified brainstem malformation characterized by specific features on neuroimaging, including a flattened ventral pons and a bulging pontine tegmentum.
  • A 3-month-old male infant exhibited classic neuroradiological signs of PTCD, along with multiple physical anomalies, such as left ocular and facial underdevelopment, hearing loss, and skeletal differences.
  • The presence of these anomalies led to the consideration that PTCD and Oculoauriculovertebral spectrum (OAVS) might have shared underlying causes in their development.

Article 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.

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Source
http://dx.doi.org/10.1016/j.braindev.2014.02.007DOI Listing

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