Abstract
Capillary malformation-arteriovenous malformation syndrome (CM-AVM) is a rare condition associated with mutations in the genes RASA1 and EPHB4. We present a challenging case of CM-AVM in a 17-month-old boy with permanent diplegia from an undiagnosed arteriovenous malformation underlying a large atypical capillary malformation over the lower thoracic spine. This case demonstrates that clinicians should have a low threshold for neuroimaging in the context of new neurologic symptoms in patients with atypical capillary malformations.
Keywords:
genetic diseases; mechanisms; vascular malformation.
© 2019 Wiley Periodicals, Inc.
MeSH terms
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Arteriovenous Fistula / diagnosis*
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Arteriovenous Fistula / diagnostic imaging
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Arteriovenous Fistula / etiology
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Arteriovenous Fistula / genetics
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Arteriovenous Malformations / complications
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Arteriovenous Malformations / diagnosis*
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Arteriovenous Malformations / diagnostic imaging
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Arteriovenous Malformations / genetics
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Capillaries / abnormalities*
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Capillaries / diagnostic imaging
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Cerebral Palsy / diagnosis*
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Cerebral Palsy / diagnostic imaging
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Cerebral Palsy / etiology
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Humans
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Infant
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Male
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Missed Diagnosis / adverse effects*
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Port-Wine Stain / complications
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Port-Wine Stain / diagnosis*
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Port-Wine Stain / diagnostic imaging
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Port-Wine Stain / genetics
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Spinal Cord Diseases / diagnosis*
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Spinal Cord Diseases / diagnostic imaging
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Spinal Cord Diseases / etiology
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Spinal Cord Diseases / genetics
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Thoracic Vertebrae
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p120 GTPase Activating Protein / genetics*
Substances
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RASA1 protein, human
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p120 GTPase Activating Protein
Supplementary concepts
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Capillary Malformation-Arteriovenous Malformation