Unilateral somatic and intracranial hypoplasia

Neuropediatrics

Volumn 28, Issue 6, 1997, Pages 341-344

  Pascual Castroviejo, I ^a   Pascual Pascual, S I ^a   Viano J ^b   Martinez V ^b  

^a HOSPITAL UNIVERSITARIO LA PAZ   (Spain)

^b Sanatorio Ntra Sra del Rosario   (Spain)

Author keywords

Cataract; Hemibody hypoplasia; Hemicerebellar hypoplasia; Hemicerebral hypoplasia; Mental retardation; Seizures

Indexed keywords

ADULT; AGENESIS; ARTICLE; BREAST HYPOPLASIA; CASE REPORT; CEREBELLUM HYPOPLASIA; CORPUS CALLOSUM; ECTODERM; FEMALE; HUMAN; MESODERM; MICROGYRIA; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL;

EID: 0030785237     PISSN: 0174304X     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2007-973729     Document Type: Article

References (27)

1. Aicardi, J., J. Lefebvre, A. Lerique-Koechlin: A new syndrome: spasm in flexion, callosal agenesis, ocular abnormalities. Electroencephalogr. Clin. Neurophysiol. 19 (1965) 609-610
2. Al-Gazali, L. I., D. Donnai, S. A. Berry, B. Say, R. F. Mueller: The oculocerebrocutaneous (Delleman) syndrome. J. Med. Genet. 25 (1988) 773-778
3. Asher, S. W., B. O. Berg: Progressive hemifacial atrophy. Report of three cases, including one observed over 43 years, and computed tomographic findings. Arch. Neurol. 36 (1982) 44-46
4. Ceballos, R., L. T. Ch'ien, R. J. Whitley, Y. W. Brands: Cerebellar hypoplasia in an infant with congenital cytomegalovirus infection. Pediatrics 57 (1976) 155-157
5. Delleman, J. W., J. W. E. Oorthuys: Orbital cyst in addition to congenital cerebral and focal dermal malformations: A new entity? Clin. Genet. 19 (1981) 191-198
6. De Souza, N., R. Chaudhuri, J. Bingham, T. Cox: MRI in cerebellar hypoplasia. Neuroradiology 36 (1994) 148-151
7. Ferguson, J. W., H. T. Hutchison, B. M. Rouse: Ocular, cerebral and cutaneous malformation: confirmation of an association. Clin. Genet. 25 (1984) 470-472
8. Hendriks, H. J. E., H. G. Brunner, T. A. M. Haagen, B. C. J. Hamel: Acrocallosal syndrome. Am. J. Med. Genet. 35 (1990) 443-446
9. Johnson, V. P., V. W. Swayze II, Y. Sato, N. C. Andreasen: Fetal alcohol syndrome: Craniofacial and central nervous system manifestations. Am. J. Med. Genet. 61 (1996) 329-339
10. Lemire, R. J., J. D. Loeser, R. W. Leech, E. C. Jr. Alvord: Normal and Abnormal Development of the Human Nervous System. Hagerstwn, Harper and Row (1975) 144-163
11. Muller, J.: Changes in cerebral sulcation in simple absence of the corpus callosum: evidence of rules controlling sulcation patterns. Can. J. Neurol. Sci. 17 (1990) 343-344
12. Njiokiktjien, C., J. Valk, G. Ramaekers: Malformation or damage of the corpus callosum? A clinical and MRI study. Brain Dev. 10 (1988) 92-99
13. Pascual-Castroviejo, I., A. Tendero, A. Martinez Bermejo, J. M. Lopez-Terradas, C. Casas: Persistence of the hypoglossal artery and partial agenesis of the cerebellum. Neuropaediatrie 6 (1975) 184-189
14. Pascual-Castroviejo, I.: Vascular and nonvascular intracranial malformations associated with external capillary hemangiomas. Neuroradiology 16 (1978) 82-84
15. Pascual-Castroviejo, I.: Vascular changes in cerebellar developmental defects. Neuroradiology 16 (1978) 58-60
16. Pascual-Castroviejo, I.: The association of extracranial and intracranial vascular malformations in children. Can. J. Neurol. Sci. 12 (1985) 139-148
17. Pascual-Castroviejo, I., J. Viaño, F. Moreno, R. Palencia, V. Martinez Fernandez, S. I. Pascual-Pascual, A. Martinez-Bermejo, J. J. García-Peñas, M. C. Roche: Hemangiomas of the head, neck, and chest with associated vascular and brain anomalies; A complex neurocutaneous syndrome. Amer. J. Neuroradiol. (AJNR) 17 (1996) 461-471
18. Sarnat, H. B.: Cerebral Dysgenesis: Embryology and Clinical Expression. New York, Oxford University Press (1992) 62-71
19. Sarnat, H. B.: Cerebral Dysgenesis: Embryology and Clinical Expression. New York, Oxford University Press (1992) 223
20. Sarnat, H. B.: Cerebral Dysgenesis: Embryology and Clinical Expression. New York, Oxford University Press (1992) 316
21. Sarnat, H. B., P. Diadori, C. L. Trevenen: Myopathy of the Proteus syndrome: Hypothesis of muscular dysgenesis. Neuromusc. Disord. 3 (1993) 293-301
22. Strefling, A. M., H. Urich: Crossed cerebellar atrophy: an oid problem revisited. Acta Neuropathol. (Berl) 57 (1982) 197-202
23. Van Bogaert, L., M. A. Rademeker: Une dysgénésie cérébelleuse chez un enfant du radium. Rev. Neurol. 93 (1955) 65-82
24. Van Dalen, J. T. W.: Hemifacial atrophy. Systemic and ophthalmologial anomalies; a review and a case report. Neuroophthalmol 6 (1986) 73-78
25. Wilson, R. D., L. Traverse, J. G. Hall, C. O. Flodmark, J. Rootman: Oculocerebrocutaneous syndrome. Am. J. Ophthalmol. 99 (1985) 142-148
26. Wood, B., J. E. Dimmick: Skeletal system. In: Dimmick, J. E., D. K. Kalousek (Eds.): Developmental Pathology of the Embryo and fetus. Philadelphia, J. B. Lippincott Company 2 (1992) 667
27. Write, V. A., R. Rootman: Eye. In: Dimmick, J. E., D. K. Kalousek (Eds.): Developmental Pathology of the Embryo and Fetus. Philadelphia, J. B. Lippincott Company (1992) 401-423