Unilateral cerebellar hypoplasia: An alteration of vascular origin?;Hipoplasia unilateral de hemisferio cerebeloso: ¿Una alteración de origen vascular?

Revista de Neurologia

Volumn 36, Issue 9, 2003, Pages 841-845

  Granados Alzamora, V ^a   Pascual Pascual, S I ^b   Pascual Castroviejo, Ignacio ^b  

^a HOSPITAL NACIONAL GUILLERMO ALMENARA IRIGOYEN   (Peru)

^b HOSPITAL UNIVERSITARIO LA PAZ   (Spain)

Author keywords

Cerebellar arteries; Cerebellum; Psychomotor retardation; Unilateral cerebellar hypoplasia

Indexed keywords

ARTERIOGRAPHY; ARTICLE; BRAIN ANGIOGRAPHY; BRAIN MALFORMATION; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; COMPUTER ASSISTED TOMOGRAPHY; CONGENITAL BLOOD VESSEL MALFORMATION; FEMALE; HUMAN; INFANT; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; PSYCHOMOTOR ACTIVITY; UNILATERAL CEREBELLAR HYPOPLASIA;

EID: 0037974309     PISSN: 02100010     EISSN: None     Source Type: Journal    
DOI: 10.33588/rn.3609.2002559     Document Type: Article

References (22)

1. Patel S, Barkovich AJ. Analysis and classification of cerebellar malformations. Am J Neuroradiol 2002; 23: 1074-87.
2. De Souza N, Chaudhuri R, Bingham J, Cox T. MRI in cerebellar hypoplasia. Neuroradiology 1994; 36: 148-51.
3. Franco E, Casado J, Díaz-Espejo C. Inicio sintomático tardío de una hipoplasia cerebelosa unilateral. Neurología 2000; 15: 261-3.
4. Amarenco P. The spectrum of cerebellar infarctions. Neurology 1991; 41: 973-9.
5. Simon M, Kafritsas D. Unilateral cerebellar hypoplasia. Clin Neuropathol 1992; 11: 71-3.
6. Pascual-Castroviejo I. Vascular and nonvascular intracranial malformations associated with external capillary hemangiomas. Neuroradiology 1978; 16: 82-4.
7. Torres-Mohedas J, Verdú A, Vidal B, Jadraque R. Presentación conjunta de hemangioma facial, malformaciones de la fosa posterior e hipoplasia carótido-(síndrome de Pascual-Castroviejo II): aportación de dos nuevos casos. Rev Neurol 2001; 32: 50-4.
8. Bélenguer-Quintana A, Aparicio-Meix JM, Quintana-Castilla A. Sindrome de Pascual-Castoviejo II: asociación de hemangioma facial, alteración de fosa posterior y cardiopatia congénita. An Esp Pediatr 2002; 57: 588-9.
9. Erdogan N, Kocakoc E, Bekar D, Ozturk O. Unilateral absence of cerebellar hemisphere: a case report. Neuroradiology 2002; 44: 49-51.
10. Altman NR, Naidich TP, Braffman BH. Posterior fossa malformations. Am J Neuroradiol 1992; 13: 691-724.
11. Bolthauser E, Steinlin M, Martín E, Deonna T. Unilateral cerebellar aplasia. Neuropediatrics 1996; 27: 50-3.
12. Ramaekers VT, Heimann G, Reul J, Thron A, Jaeken J. Genetic disorders and cerebellar structural abnormalities in childhood. Brain 1997; 120: 1739-51.
13. Pascual-Castroviejo I, Pascual-Pascual SI, Viaño J, Martínez V. Unilateral somatic and intracranial hypoplasia. Neuropediatrics 1997; 28: 341-4.
14. Pascual-Castroviejo I, Santolaya JM, Tendero A. Development defects of the cerebellum. A radiological and anatomic investigation. Acta Radiol 1975; 347: 553-60.
15. Johnsen S, Tarby T, Lewis KS. Cerebellar infarction: An unrecognized complication of very low birthweight. J Child Neurol 2002; 17: 320-4.
16. Wang PJ, Maeda Y, Izumi T, Yajima K, Hara M, Kubayashi N, et al. An association of sub-total cerebellar agenesis with organoid naevus a possible new variety of neurocutaneous syndrome. Brain Dev 1983; 5: 503-8.
17. Mizuno Y, Kurokawa T, Numaguchi Y, Goya N. Facial haemangioma with cerebrovascular anomalies and cerebellar hypoplasia. Brain Dev 1982; 4: 375-8.
18. Campistol J. Nuevos conocimientos en la fisiopatología del cerebelo. Rev Neurol 2002; 35: 231-5.
19. Bertini E, Campos-Castelló J. Ataxias congénitas de origen genético con anomalías estructurales del cerebelo. Rev Neurol 1999; 28: 63-8.
20. Ross ME, Swanson K, Dobyns WB. Lyssencephaly with cerebellar hypoplasia (LCH): a heterogeneous group of cortical malformations. Neuropediarics 2001; 32: 256-63.
21. Samat HB, Benjamín DR, Sibert JR, Kletter B, Cheyette SR. Agenesis of the mesencephalon and metencephalon with cerebellar hypoplasia: putative mutation in the EN2 gene - report of 2 cases in early infancy. Pediatr Dev Pathol 2002; 5: 54-68.
22. Hiyasat D, Dahyyat MA, Ajlounis S, Mubaidin AF, Till M, Hadidi A, et al. Cerebellar hypoplasia, hypergonadotrophic hypogonadism, retinitis pigmentosa, alopecia, microcephaly, psicomotor retardation, and short stature: D-CHRAMPS syndrome. Eur J Pediatr 2002; 161: 170-2.