Lateral meningocele syndrome


Meningocele

Protrusion of the meninges through a defect of the vertebral column.


合計: 5

                       


（表示件数）
PMID (PMCID)
23962060
 MALE Infant
Lehman syndrome: a new syndrome for pierre robin sequence.
Correia-Sa I, Horta R, Neto T, Amarante J, Marques M.
Cleft Palate Craniofac J. 2015;52(3):369-72.
Lehman syndrome, or lateral meningocele syndrome, is characterized by facial dysmorphism, multiple lateral meningoceles, and skeletal abnormalities.
23962060
 MALE Infant
Lehman syndrome: a new syndrome for pierre robin sequence.
Correia-Sa I, Horta R, Neto T, Amarante J, Marques M.
Cleft Palate Craniofac J. 2015;52(3):369-72.
Later, multiple lateral meningoceles were identified, and a diagnosis of Lehman syndrome was made.
25394726
(5589071)
 MALE Child
Truncating mutations in the last exon of NOTCH3 cause lateral meningocele syndrome.
Gripp KW, Robbins KM, Sobreira NL, Witmer PD, Bird LM, Avela K, Makitie O, Alves D, Hogue JS, Zackai EH, Doheny KF, Stabley DL, Sol-Church K.
Am J Med Genet A. 2015;167A(2):271-81.
Lateral meningocele syndrome (LMS, OMIM%130720), also known as Lehman syndrome, is a very rare skeletal disorder with facial anomalies, hypotonia and meningocele-related neurologic dysfunction.
24311540
 FEMALE Middle Aged
Late diagnosis of lateral meningocele syndrome in a 55-year-old woman with symptoms of joint instability and chronic musculoskeletal pain.
Castori M, Morlino S, Ritelli M, Brancati F, De Bernardo C, Colombi M, Grammatico P.
Am J Med Genet A. 2014;164A(2):528-34.
Lateral meningocele syndrome (LMS) is a rare hereditary connective tissue disorder characterized by pan-spinal meningoceles, specific facial dysmorphism, skeletal and soft tissue abnormalities, and hypotonia and/or muscle weakness.
8574426
 MALE Adult
Multiple lateral meningoceles, distinctive facies and skeletal anomalies: a new case of Lehman syndrome.
Philip N, Andrac L, Moncla A, Sigaudy S, Zanon N, Lena G, Choux M.
Clin Dysmorphol. 1995;4(4):347-51.
Multiple lateral meningoceles, distinctive facies and skeletal anomalies: a new case of Lehman syndrome.