Cerebral hemorrhage in monozygotic twins with hereditary hemorrhagic telangiectasia: case report and hemorrhagic risk evaluation

Author:

Rattani Abbas1,Dewan Michael C.2,Hannig Vickie3,Naftel Robert P.2,Wellons John C.2,Jordan Lori C.4

Affiliation:

1. School of Medicine, Meharry Medical College, Nashville;

2. Division of Pediatric Neurosurgery, Department of Neurological Surgery, and

3. Divisions of Medical Genetics and Genomic Medicine and

4. Pediatric Neurology, Department of Pediatrics, Vanderbilt University Medical Center, Monroe Carell Jr. Children’s Hospital at Vanderbilt, Nashville, Tennessee

Abstract

The authors present a case of monozygotic twins with hereditary hemorrhagic telangiectasia (HHT) who experienced cerebral arteriovenous malformation (AVM) hemorrhage at a very young age. The clinical variables influencing HHT-related AVM rupture are discussed, and questions surrounding the timing of screening and intervention are explored. This is only the second known case of monozygotic HHT twins published in the medical literature, and the youngest pair of first-degree relatives to experience AVM-related cerebral hemorrhage. Evidence guiding the screening and management of familial HHT is lacking, and cases such as this underscore the need for objective and validated protocols.

Publisher

Journal of Neurosurgery Publishing Group (JNSPG)

Subject

General Medicine

Reference68 articles.

1. Cerebrovascular manifestations of hereditary hemorrhagic telangiectasia;Brinjikji;Stroke,2015

2. Hereditary haemorrhagic telangiectasia: current views on genetics and mechanisms of disease;Abdalla;J Med Genet,2006

3. Hereditary hemorrhagic telangiectasia;Guttmacher;N Engl J Med,1995

4. Brain vascular malformation consortium: overview, progress and future directions;Akers;J Rare Disord,2013

5. Hereditary hemorrhagic telangiectasia;Guttmacher;N Engl J Med,1995

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