1979
DOI: 10.2214/ajr.132.1.130
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Agenesis of the internal carotid artery with a primitive transsellar communicating artery

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Cited by 31 publications
(6 citation statements)
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“…ICA agenesis is a rare congenital anomaly, reported in less than 0.01% of the population. The spectrum of findings ranges from agenesis (complete absence of the ICA and carotid canal) to aplasia (absence of parts of the ICA and of the carotid canal) and hypoplasia (narrowing of the ICA and carotid canal) ( 1 - 4 ) .…”
mentioning
confidence: 99%
“…ICA agenesis is a rare congenital anomaly, reported in less than 0.01% of the population. The spectrum of findings ranges from agenesis (complete absence of the ICA and carotid canal) to aplasia (absence of parts of the ICA and of the carotid canal) and hypoplasia (narrowing of the ICA and carotid canal) ( 1 - 4 ) .…”
mentioning
confidence: 99%
“…Thirty-six other cases of congenital absence of ICA with intercavernous anastomosis were identified in the literature. 2,434 Age and gender information was not given in one case. 14 We documented sex, laterality of the lesion, age at diagnosis, and presenting clinical signs/symptoms.…”
Section: Methodsmentioning
confidence: 99%
“…Padget 11 noted that the primitive maxillary artery originates from the cavernous ICA lateral to the base of the Rathke pouch in the 3-to 4-mm embryo and has the primary role of supplying the prosencephalon and the optic vesicle. Janicki et al 6 opined that this vessel is most likely incorporated into the inferior hypophyseal artery. Quint et al 12 suggested that insult to the ICA during development might result in compensatory hypertrophy between clival branches of the left and right ICAs, thus forming an intercavernous connection.…”
Section: Potential Embryologymentioning
confidence: 99%