Surgical treatment of a congenital dacryocystocele by means of microdebrider marsupialization in a newborn [PDF]
Clinical Case Reports, 2021 Congenital dacryocystocele is a rare clinical condition, more commonly unilateral, secondary to the defective canalization of the nasolacrimal duct. In case of failure of conservative treatment, surgical marsupialization is recommended.
Domenico diFuria +5 more
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Outcomes of lacrimal probing surgery as the first option in the treatment of congenital dacryocystocele [PDF]
Therapeutic Advances in Ophthalmology, 2021 Purpose: To determine the demographic and clinical characteristics of newborn patients who underwent lacrimal probing surgical intervention with or without the marsupialization of intranasal cysts as the primary management for dacryocystocele treatment ...
Cetin Akpolat +5 more
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Process of spontaneous resolution in the conservative management of congenital dacryocystocele [PDF]
Clinical Ophthalmology, 2014 Masashi Mimura,1,2 Mari Ueki,1 Hidehiro Oku,1 Bunpei Sato,2 Tsunehiko Ikeda11Department of Ophthalmology, Osaka Medical College, Takatsuki, 2Department of Ophthalmology, Osaka Kaisei Hospital, Osaka, JapanPurpose: To assess efficacy of the conservative ...
Mimura M, Ueki M, Oku H, Sato B, Ikeda T
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Risk Factors and Clinical Outcomes of Secondary Infection in Congenital Dacryocystocele [PDF]
Ophthalmology and TherapyIntroduction Congenital dacryocystocele (CD) represents a rare yet clinically significant subtype of congenital nasolacrimal duct obstruction. It carries a substantial risk of severe secondary infection, yet its risk factors have not been fully ...
Yanhong Ren +8 more
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Routine 36-week scan: diagnosis of fetal abnormalities. [PDF]
Ultrasound Obstet GynecolABSTRACT Objectives To investigate further the incidence and types of fetal abnormality identified at a routine 36‐week ultrasound examination, which had not been diagnosed in previous scans at 20 weeks and 12 weeks' gestation, and to report the fetal abnormalities that are diagnosed only postnatally.
Syngelaki A +5 more
europepmc +2 more sources
Congenital dilatation of the nasolacrimal sac (Dacryocystocele): Case report [PDF]
Journal of Family Medicine and Primary Care, 2019 Congenital dacryocystoceles are usually diagnosed in the third trimester by parental ultrasound as a cystic lesion adjacent to the medial and inferior aspects of the fetal orbit.
Sakiyeva Kanshaiym +4 more
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An unusual twinning moment – A rare occurrence of unilateral congenital dacryocystocele in a pair of monozygotic identical twins [PDF]
Indian Journal of Ophthalmology, 2022 Shruthy V Ramesh +6 more
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Masquerades of Acquired Dacryocystocele [PDF]
Clinical Ophthalmology, 2020 Nandini Bothra, Richa Dharap Wagh, Mohammad Javed Ali Govindram Seksaria Institute of Dacryology, L.V. Prasad Eye Institute, Hyderabad 500034, Telangana, IndiaCorrespondence: Nandini BothraGovindram Seksaria Institute of Dacryology, L.V.
Bothra N, Wagh RD, Ali MJ
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Endoscopic endonasal dacryocystectomy [PDF]
American Journal of Ophthalmology Case ReportsPurpose: To report an exceptionally rare instance of Endoscopic endonasal dacryocystectomy. Observations: Dacryocystectomy (DCT), a procedure of surgical extirpation of the lacrimal sac is normally approached by an external route.
Juhi Daga, Mohammad Javed Ali
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Novel KIF26A variants associated with pediatric intestinal pseudo-obstruction (PIPO) and brain developmental defects. [PDF]
Clin GenetThis study identifies novel biallelic KIF26A variants in three patients with congenital hydrocephalus and intestinal obstruction. Using 3D protein modeling, we reveal that missense variants cause significant structural destabilization of the KIF26A protein. Additionally, histopathology data show aganglionosis and elevated acetylcholinesterase activity,
Nosrati MSS +24 more
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