Spontaneous intracranial hemorrhage and multiple intracranial aneurysms in a patient with Roberts/SC phocomelia syndrome

Author:

Wang Anthony C.1,Gemmete Joseph J.2,Keegan Catherine E.3,Witt Cordelie E.1,Muraszko Karin M.1,Than Khoi D.1,Maher Cormac O.1

Affiliation:

1. Departments of Neurosurgery,

2. Radiology, and

3. Pediatrics and Communicable Diseases, University of Michigan, Ann Arbor, Michigan

Abstract

Roberts/SC phocomelia syndrome (RBS) is a rare but distinct genetic disorder with an autosomal recessive inheritance pattern. It has been associated with microcephaly, craniofacial malformation, cavernous hemangioma, encephalocele, and hydrocephalus. There are no previously reported cases of RBS with intracranial aneurysms. The authors report on a patient with a history of RBS who presented with a spontaneous posterior fossa hemorrhage. Multiple small intracranial aneurysms were noted on a preoperative CT angiogram. The patient underwent emergency craniotomy for evacuation of the hemorrhage. A postoperative angiogram confirmed the presence of multiple, distal small intracranial aneurysms.

Publisher

Journal of Neurosurgery Publishing Group (JNSPG)

Subject

General Medicine

Cited by 8 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Complex cerebrovascular diseases in Roberts syndrome caused by novel biallelic ESCO2 variations;Molecular Genetics & Genomic Medicine;2023-03-31

2. Intracranial Aneurysms and Subarachnoid Hemorrhage;Contemporary Medical Imaging;2023

3. Intracranial Aneurysms and Subarachnoid Hemorrhage;Handbook of Cerebrovascular Disease and Neurointerventional Technique;2018

4. Roberts syndrome – An isolated case;Medicina Universitaria;2017-04

5. Evolution of Management of Intracranial Aneurysms in Children;Journal of Child Neurology;2015-10-29

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