1985
DOI: 10.1001/archopht.1985.01050040087025
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Congenital Lacrimal Fistulas

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Cited by 58 publications
(37 citation statements)
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“…Congenital lacrimal fistula are uncommon developmental anomalies of the nasolacrimal excretory system with an estimated incidence of one in , 2000 births [3,10,11] and occasionally can be inherited in an autosomal dominant [1, 4,7,11] or recessive pattern [1, 3,4,9]. They are usually unilateral [2, 3,5,12] but familial cases are associated with higher incidence of bilaterally [4,9].…”
Section: Discussionsupporting
confidence: 40%
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“…Congenital lacrimal fistula are uncommon developmental anomalies of the nasolacrimal excretory system with an estimated incidence of one in , 2000 births [3,10,11] and occasionally can be inherited in an autosomal dominant [1, 4,7,11] or recessive pattern [1, 3,4,9]. They are usually unilateral [2, 3,5,12] but familial cases are associated with higher incidence of bilaterally [4,9].…”
Section: Discussionsupporting
confidence: 40%
“…The fistulae can originate from common canaliculus, lacrimal sac or nasolacrimal duct of skin [4][5][6][7]. In 1675, the first description of congenital lacrimal sac was reported by Rasor [7][8][9].…”
Section: Introductionsupporting
confidence: 46%
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“…In some cases, these may result from a secondary cause. However, most cases are congenital; therefore, congenital LF is the most accurate term for this condition [1]. The incidence of congenital LF is estimated to be 1 in 2000 births, and occasionally LF can be inherited in an autosomal dominant or autosomal recessive pattern [3][4][5].…”
Section: Introductionsupporting
confidence: 42%
“…Lacrimal fistulas (LFs), also known as lacrimal anlage ducts, are supernumerary lacrimal canaliculi that connect the skin to the common canaliculus or the lacrimal sac [1,2]. In some cases, these may result from a secondary cause.…”
Section: Introductionsupporting
confidence: 39%