Meckel-Gruber syndrome in association with an occipital meningocele

Pediatric Neurosurgery

Volumn 42, Issue 5, 2006, Pages 333-334

  Walsh, Michael ^a   Graupman, Patrick ^a,b  

^a UNIVERSITY OF VERMONT COLLEGE OF MEDICINE   (United States)

^b UNIVERSITY OF VERMONT   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CESAREAN SECTION; DISEASE ASSOCIATION; FETUS; FETUS ECHOGRAPHY; GESTATIONAL AGE; HUMAN; MALE; MECKEL SYNDROME; MENINGOCELE; NEUROSURGERY; NUCLEAR MAGNETIC RESONANCE IMAGING; PATIENT REFERRAL; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SYNDROME DELINEATION;

ABNORMALITIES, MULTIPLE; ENCEPHALOCELE; FATAL OUTCOME; HUMANS; INFANT, NEWBORN; MALE; MENINGOCELE; OCCIPITAL LOBE; POLYCYSTIC KIDNEY DISEASES; SYNDROME; ULTRASONOGRAPHY, PRENATAL;

EID: 33747147746     PISSN: 10162291     EISSN: None     Source Type: Journal    
DOI: 10.1159/000094074     Document Type: Article

References (3)

1. Farag TI, Usha R, Uma R, Mady SA, al-Nagdy K, el-Badramany MH: Phenotypic variability in Meckel-Gruber syndrome. Clin Genet 1990;38:176-179.
2. Gazioglu N, Vural M, Seckin MS, Tuysuz B, Akpir E, Kuday C, Ilikkan B, Erginel A, Cenani A: Meckel-Gruber syndrome. Childs Nerv Syst 1998;14:142-145.
3. Morgan NV, Gissen P, Sharif SM, Baumber L, Sutherland J, Kelly DA, Aminu K, Bennett CP, Woods CG, Mueller RF, Trembath RC, Maher ER, Johnson CA: A novel locus for Meckel-Gruber syndrome, MKS3, maps to chromosome 8q24. Hum Genet 2002;111:456-461.