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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease tolosa hunt syndrome
Comorbidity C0040053|thrombosis
Sentences 1
PubMedID- 24476631 This report describes a very unusual case of fusiform aneurysms of both icas in a caucasian nf1 patient, with a new pathogenic intragenic heterozygous deletion of the nf1 gene, presenting at age 22 years with tolosa-hunt syndrome, because of partial thrombosis of the left giant intracavernous aneurysm.

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