Name: PubCaseFinder
License: http://creativecommons.org/licenses/by/2.1/jp/
Keywords: PubCaseFinder,PCF,Rare Disease,Phenotype,Gene,Match,Assist

Lateral meningocele syndrome

Lateral spinal meningocele

Protrusion of the arachnoid and dura through spinal foramina.

Total: 2

(per page)

PMID (PMCID)
26754023	MALE
	Lateral meningocele (Lehman) syndrome: A child with a novel NOTCH3 mutation.
	Ejaz R, Qin W, Huang L, Blaser S, Tetreault M, Hartley T, Boycott KM, Carter MT. Am J Med Genet A. 2016;170A(4):1070-5.
	Lateral meningocele syndrome (LMS), or Lehman syndrome, is a rare disorder characterized by multiple lateral spinal meningoceles, distinctive facial features, joint hypermobility and hypotonia, along with skeletal, cardiac, and urogenital anomalies.
26754023	MALE
	Lateral meningocele (Lehman) syndrome: A child with a novel NOTCH3 mutation.
	Ejaz R, Qin W, Huang L, Blaser S, Tetreault M, Hartley T, Boycott KM, Carter MT. Am J Med Genet A. 2016;170A(4):1070-5.
	Lateral meningocele syndrome (LMS), or Lehman syndrome, is a rare disorder characterized by multiple lateral spinal meningoceles, distinctive facial features, joint hypermobility and hypotonia, along with skeletal, cardiac, and urogenital anomalies.