Simultaneous development of pheochromocytomas in prepubertal siblings with von Hippel-Lindau syndrome - 01/09/11
Doi : 10.1067/mpd.2002.123279
Sherry Lynn Franklin, MD, Graeme Eisenhofer, PhD, Mitchell E. Geffner, MD
From the Division of Endocrinology, Department of Pediatrics, Mattel Children's Hospital at UCLA, Los Angeles, California, and the National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland.
Abstract |
We report 2 siblings with a known von Hippel-Lindau mutation who simultaneously developed asymptomatic pheochromocytomas at significantly younger ages than are typically seen in this setting. (J Pediatr 2002;140:625-8)
Le texte complet de cet article est disponible en PDF. | Supported in part by a Nutrition Center National Institutes of Health Institutional National Research Service Award training grant #DK07688-08, and a grant from the Carolan Foundation. |
© 2002
Mosby, Inc. Tous droits réservés.
Vol 140 - N° 5
P. 625-628 - mai 2002 Retour au numéro
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