Pontine tegmental cap dysplasia: a novel brain malformation with a defect in axonal guidance

• Published in: Brain (London, England : 1878) Vol. 130; no. 9; pp. 2258 - 2266
• Main Authors: Barth, Peter G., Majoie, Charles B., Caan, Matthan W.A., Weterman, Marian A.J., Kyllerman, Marten, Smit, Leo M.E., Kaplan, Richard A., Haas, Richard H., Baas, Frank, Cobben, Jan-Maarten, Poll-The, Bwee Tien
• Format: Journal Article
• Language: English
• Published: England Oxford University Press 01.09.2007; Oxford Publishing Limited (England)
• Subjects: axonal guidance; Axons - pathology; Brain - pathology; Cerebellum - abnormalities; Cerebellum - pathology; Child, Preschool; deleted in colorectal cancer; DNA Mutational Analysis; Female; Genes, DCC - genetics; Humans; Infant; Magnetic Resonance Imaging; Male; molar tooth complex; Nerve Growth Factors - genetics; Netrin-1; Pons - abnormalities; Pons - pathology; pontine hypoplasia; Syndrome; Tumor Suppressor Proteins - genetics; deleted in colorectal cancer; molar tooth complex; pontine hypoplasia; axonal guidance; netrin 1
• ISSN: 0006-8950; 1460-2156
• DOI: 10.1093/brain/awm188

Four unrelated children are described with an identical brainstem and cerebellar malformation on MRI. The key findings are: vermal hypoplasia, subtotal absence of middle cerebellar peduncles, flattened ventral pons, vaulted pontine tegmentum, molar tooth aspect of the pontomesencephalic junction and absent inferior olivary prominence. Peripheral hearing impairment is present in all. Variable findings are: horizontal gaze palsy (1/4), impaired swallowing (2/4), facial palsy (3/4), bilateral sensory trigeminal nerve involvement (1/4), ataxia (2/4). Bony vertebral anomalies are found in 3/4. Additional MR studies in one patient using diffusion tensor imaging (DTI) with colour coding and fibre tracking revealed an ectopic transverse fibre bundle at the site of the pontine tegmentum and complete absence of transverse fibres in the ventral pons. The combined findings indicate an embryonic defect in axonal growth and guidance. Phenotypic analogy to mice with homozygous inactivation of Ntn1 encoding the secreted axonal guidance protein netrin1, or Dcc encoding its receptor Deleted in Colorectal Cancer led us to perform sequence analysis of NTN1 and DCC in all the patients. No pathogenic mutations were found. For the purpose of description the name ‘pontine tegmental cap dysplasia’ (PTCD) is proposed for the present malformation, referring to its most distinguishing feature on routine MRI.