Syringomyelia in VACTERL-H association: a new neurological feature in an adult patient-Reference-Cited by-同舟云学术

Syringomyelia in VACTERL-H association: a new neurological feature in an adult patient

Published:2015-07-21 Issue:2 Volume:116 Page:229-231
ISSN:0300-9009
Container-title:Acta Neurologica Belgica
language:en
Short-container-title:Acta Neurol Belg

Author:

Salinas-Torres Victor M.

Publisher

Springer Science and Business Media LLC

Subject

Neurology (clinical),General Medicine

Link

http://link.springer.com/content/pdf/10.1007/s13760-015-0513-1.pdf

Reference7 articles.

1. Salinas-Torres VM, Pérez-García N, Pérez-García G (2015) Clinical, cytogenetic, environmental and inheritance findings in Mexican neonates with VACTERL association. Indian J Pediatr 82:84–88

2. Online Mendelian Inheritance in Man® Johns Hopkins University, Baltimore, MD. MIM Numbers: 276950 and 314390: 04/24/2015. http://www.ncbi.nlm.nih.gov/omim . Accessed 24 Apr 2015

3. Salinas-Torres VM, Ramos-Márquez ME, Serra-Ruiz L, Angulo-Castellanos E (2012) Unusual branchial arch, dermoepidermal and nervous system anomalies in a neonate with VACTERL-H syndrome. Arch Argent Pediatr 110:e67–e71

4. Salinas-Torres VM, Ramos-Márquez ME, Angulo-Castellanos E (2013) VACTERL-H association with tibial agenesis. Expansion of the clinical phenotype? An Pediatr (Barc) 79:125–127

5. Friedland-Little JM, Hoffmann AD, Ocbina PJ, Peterson MA, Bosman JD, Chen Y, Cheng SY, Anderson KV, Moskowitz IP (2011) A novel murine allele of Intraflagellar Transport Protein 172 causes a syndrome including VACTERL-like features with hydrocephalus. Hum Mol Genet 20:3725–3737

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