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glomus tumor/tyrosine
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Additional glomangioma families link to chromosome 1p: no evidence for genetic heterogeneity.
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Venous malformations are a common abnormality of the vasculature that may occur sporadically or, more rarely, as an autosomal dominant trait. One familial form of venous malformations has previously been linked to chromosome 9p. Mutations in the gene encoding Tie2, an endothelial specific receptor
A gene for inherited cutaneous venous anomalies ("glomangiomas") localizes to chromosome 1p21-22.
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Venous malformations (VMs) are localized defects of vascular morphogenesis. They can occur in every organ system, most commonly in skin and muscle. They can cause pain and bleeding, and in some critical locations they can be life threatening. Usually venous anomalies occur sporadically, but families
Hypertension and a tumor of the glomus jugulare region. Evidence for epinephrine biosynthesis.
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Glomus jugulare tumors have been reported to secrete norepinephrine and cause severe hypertension with features similar to pheochromocytoma. In contrast, epinephrine secretion has not been observed in these neoplasms. This has been attributed to the absence of the norepinephrine-methylating enzyme,
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