Volume 46, Issue 6 pp. 614-616
Case Report

Pulmonary outcome of alport syndrome with familial diffuse esophageal leiomymatosis

Galit Livnat MD

Galit Livnat MD

Pediatric Pulmonary Unit, Meyer Children's Hospital, Haifa, Israel

Rambam Health Care Campus, The Bruce Rappaport Faculty of Medicine, Technion Israel Institute of Technology, Haifa, Israel

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Lael Anson Best MD

Lael Anson Best MD

Rambam Health Care Campus, The Bruce Rappaport Faculty of Medicine, Technion Israel Institute of Technology, Haifa, Israel

Department of General Thoracic Surgeries, Rambam Medical Center, Haifa, Israel

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Ludmila Guralnik MD

Ludmila Guralnik MD

Rambam Health Care Campus, The Bruce Rappaport Faculty of Medicine, Technion Israel Institute of Technology, Haifa, Israel

Department of Clinical Imaging, Rambam Medical Center, Haifa, Israel

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Lea Bentur MD

Corresponding Author

Lea Bentur MD

Pediatric Pulmonary Unit, Meyer Children's Hospital, Haifa, Israel

Rambam Health Care Campus, The Bruce Rappaport Faculty of Medicine, Technion Israel Institute of Technology, Haifa, Israel

Pediatric Pulmonary Unit, Rambam Medical Center, Meyer Children's Hospital, Haifa, Israel.Search for more papers by this author
First published: 31 January 2011
Citations: 2

Abstract

X-linked Alport syndrome is associated in some families with diffuse leiomyomatosis. We describe herein, the pulmonary complications and outcome of three family members (mother, daughter, and son). The three underwent esophagectomy at different ages (22 years, three years, and 15 months respectively). Their current forced expiratory volume in the first second (FEV1) ranged from 33% in the mother to 60% in the daughter and 97% in the son. It is suggested that earlier intervention may lead to improved pulmonary function tests. Pediatr. Pulmonol. 2011; 46:614–616. © 2011 Wiley-Liss, Inc.

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