Cerebral arteriovenous malformation in Noonan's syndrome
- 1 January 1992
- journal article
- case report
- Published by Oxford University Press (OUP)
- Vol. 68 (795) , 37-40
- https://doi.org/10.1136/pgmj.68.795.37
Abstract
Summary: Noonan's syndrome involves the association of multiple congenital abnormalities including neck webbing, pectus excavatum, facial anomalies with a variety of cardiac defects. In this paper the association of Noonan's syndrome with a large cerebral arteriovenous malformation is reported. Congenital cerebrovascular abnormalities are not a recognized feature of the syndrome. The paper also reviews previous reports of neurological associations with Noonan's syndrome, the commonest being mild intellectual impairment and ptosis.Keywords
This publication has 15 references indexed in Scilit:
- Evidence that the “neurofibromatosis‐Noonan syndrome” is a variant of von Recklinghausen neurofibromatosisAmerican Journal of Medical Genetics, 1987
- New multiple congenital anomalies/mental retardation syndrome with cardio‐facio‐cutaneous involvement—the CFC syndromeAmerican Journal of Medical Genetics, 1986
- Noonan phenotype associated with neurofibromatosisAmerican Journal of Medical Genetics, 1985
- Chiari (type 1) malformation and syringomyelia in a patient with Noonan's syndrome.Journal of Neurology, Neurosurgery & Psychiatry, 1982
- Unusual combination of congenital heart lesions in a child with Noonan's syndromePediatric Cardiology, 1982
- Zerebrale Anomalien bei Noonan-SyndromKlinische Padiatrie, 1980
- Noonan's SyndromeAmerican Journal of Diseases of Children, 1979
- An evaluation of the possible association of malignant hyperpyrexia with the Noonan syndrome using serum creatine phosphokinase levelsThe Journal of Pediatrics, 1975
- The Ullrich-Noonan Syndrome (Turner Phenotype)Archives of Pediatrics & Adolescent Medicine, 1974
- Hypertelorism With Turner PhenotypeAmerican Journal of Diseases of Children, 1968