Autosomal dominant occipital cephalocele

Neurology

Volumn 62, Issue 10, 2004, Pages 1888-1890

  Bassuk, Alexander G ^a,c   McLone, David ^b   Bowman, Robin ^b   Kessler, John A ^a  

^a NORTHWESTERN UNIVERSITY   (United States)

^b NORTHWESTERN UNIVERSITY   (United States)

^c CHILDREN'S MEMORIAL HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BIRTH INJURY; BRAIN HERNIA; BRAIN RADIOGRAPHY; CASE REPORT; CLINICAL FEATURE; CONSANGUINEOUS MARRIAGE; DEVELOPMENTAL BIOLOGY; FAMILIAL DISEASE; FEMALE; HUMAN; MALE; NEUROLOGIC EXAMINATION; NEWBORN; OCCIPITAL CEPHALOCELE; OCCIPITAL CORTEX; PENETRANCE; PRIORITY JOURNAL; SCHOOL CHILD; VIET NAM;

EID: 2442710207     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.WNL.0000125255.90915.5C     Document Type: Article

References (10)

1. McLone DG. Encephaloceles. In: Kaye AH, Black PM, eds. Operative neurosurgery. London: Harcourt, 2000;1343-1352.
2. Martinez-Lage JF, Martinez Robledo A, Poza M, Sola J. Familial occurrence of atretic cephaloceles. Pediatr Neurosurg 1996;25:260-264.
3. Hsia YE, Bratu M, Herbordt A. Genetics of the Meckel syndrome (dysencephalia splanchnocystica). Pediatrics 1971;48:237-247.
4. Hirsch JF, Pierre-Kahn A, Renier D, Sainte-Rose C, Hoppe-Hirsch E. The Dandy-Walker malformation. A review of 40 cases. J Neurosurg 1984;61:515-522.
5. Williams RS, Swisher CN, Jennings M, Ambler M, Caviness VS, Jr. Cerebro-ocular dysgenesis (Walker-Warburg syndrome): neuropathologic and etiologic analysis. Neurology 1984;34:1531-1541.
6. Edwards BO, Jr., Fischer AQ, Flannery DB. Joubert syndrome: early diagnosis by recognition of the behavioral phenotype and confirmation by cranial sonography. J Child Neurol 1988;3:247-249.
7. Aleksic S, Budzilovich G, Greco MA, Epstein F, Feigin I, Pearson J. Encephalocele (cerebellocele) in the Goldenhar-Gorlin syndrome. Eur J Pediatr 1983;140:137-138.
8. Cook GR, Knobloch WH. Autosomal recessive vitreoretinopathy and encephaloceles. Am J Ophthalmol 1982;94:18-25.
9. Freeman MV, Williams DW, Schimke RN, Temtamy SA, Vachier E, German J. The Roberts syndrome. Birth Defects: Original Article Series 1974;10:87-95.
10. Holmes LB. Current concepts in genetics. Congenital malformations. N Engl J Med 1976;295:204-207.