CVA with Neurofibromatosis Type I

J Gordon Millichap

doi:10.15844/pedneurbriefs-6-7-9

CVA with Neurofibromatosis Type I

Pediatric Neurology Briefs

Volume 6 (1992): Issue 7

By: J Gordon Millichap

Open Access

|Jul 1992

Abstract

A two year old developmentally delayed girl with neurofibromatosis type I and a sudden onset of left sided hemiparesis is reported from the Children’s National Medical Center and George Washington University School of Medicine, Washington, D.C.

References

Gorelick MH Powell CM Rosenbaum KN Saal HM Conry J Fitz CR Progressive occlusive cerebrovascular disease in a patient with neurofibromatosis type 1 Clin Pediatr 1992 May 31 5 313 315 10.1177/000992289203100511 1582101
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Hofman KJ Boehm CD Familial neurofibromatosis type 1: clinical experience with DNA testing J Pediatr 1992 Mar 120 3 394 398 10.1016/S0022-3476(05)80903-5 1347082
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-6-7-9 | Journal eISSN: 2166-6482

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Language: English

Page range: 54 - 55

Published on: Jul 1, 1992

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Neurofibromatosis Type I,

Cerebral Angiography,

Moyamoya

© 1992 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 6 (1992): Issue 7