Familial Dandy-Walker malformation and leukodystrophy

Pediatric Neurology

Volumn 16, Issue 4, 1997, Pages 326-328

  Humbertclaude, Véronique T ^a   Coubes, Philippe A ^b   Leboucq, Nicolas ^c   Echenne, Bernard B ^a  

^a HÔPITAL SAINT ELOI   (France)

^b Service de Neurochirurgie   (France)

^c GUI DE CHAULIAC HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CASE REPORT; CHILD; DANDY WALKER SYNDROME; EVOKED AUDITORY RESPONSE; EVOKED VISUAL RESPONSE; FAMILIAL DISEASE; FEMALE; HUMAN; INFANT; LEUKODYSTROPHY; MALE; MUSCLE BIOPSY; NERVE BIOPSY; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL;

BRAIN DISEASES; CRANIAL FOSSA, POSTERIOR; CYSTS; DANDY-WALKER SYNDROME; FEMALE; HUMANS; INFANT; LEUKOENCEPHALOPATHY, PROGRESSIVE MULTIFOCAL; MAGNETIC RESONANCE IMAGING; MALE;

EID: 0030753899     PISSN: 08878994     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0887-8994(97)00027-1     Document Type: Article

References (6)

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3. Kyllerman M, Blomstrand S, Mänsson JE, Conradi NG, Hindmarsh T. Central nervous system malformations and white matter changes in pseudo-neonatal adrenoleukodystrophy. Neuropediatrics 1990;21:199-20.
4. Pintos-Morell G, Naranjo MA, Artigas M, et al. Molybdenum cofactor deficiency associated with Dandy-Walker malformation. J Inher Metab Dis 1995;18:86-7.
5. Holzbach U, Hanefeld F, Helms G, Hänicke W, Frahm J. Localized proton magnetic resonance spectroscopy of cerebral abnormalities in children with carbohydrate-deficient glycoprotein syndrome. Acta Paediatr 1995;84:781-6.
6. Di Rocco M, Leveratto L, Cama A, Bado M, Tortori-Donati P, Borrone C. Report on a patient with congenital muscular dystrophy, hydrocephalus, Dandy-Walker malformation and leukodystrophy. Genet Couns 1993;4:295-8.