✦ LIBER ✦

Excision of congenital nasolacrimal duct cyst with powered instrumentation

✍ Scribed by Norman R. Friedman; Margaret Luck; Victor I. Scapa

Publisher: John Wiley and Sons
Year: 2010
Tongue: English
Weight: 81 KB
Volume: 121
Category: Article
ISSN: 0023-852X
DOI: 10.1002/lary.21158

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Congenital cyst of the common bile-duct:

Congenital cyst of the common bile-duct: With report of two cases

✍ John Morley 📂 Article 📅 1923 🏛 John Wiley and Sons 🌐 English ⚖ 548 KB

Balloon dacryocystoplasty and monocanali

Balloon dacryocystoplasty and monocanalicular intubation with Monoka tubes in the treatment of congenital nasolacrimal duct obstruction

✍ Yu Hsun Huang; Shu Lang Liao; Luke L-K Lin 📂 Article 📅 2009 🏛 Springer-Verlag 🌐 English ⚖ 160 KB

Cystic lymphangioma of the pancreas with

Cystic lymphangioma of the pancreas with congenital intrahepatic duct dilatation and choledochal cyst

✍ Yao Wang; Shao-Shan Tang; Ying Ma 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 174 KB

## Abstract Cystic lymphangioma of the pancreas is an extremely rare benign tumor of lymphatic origin. We report on a 68‐year‐old woman who had experienced epigastric abdominal distension and nausea for over 1 year. Sonography revealed a cystic‐solid mixed mass in the head of pancreas, with intrahe

Efficacy of probing for children with co

Efficacy of probing for children with congenital nasolacrimal duct obstruction: a retrospective study using fluorescein dye disappearance test and lacrimal sac echography

✍ Piero Steindler; Enrico Mantovani; Carlo Incorvaia; Francesco Parmeggiani 📂 Article 📅 2008 🏛 Springer-Verlag 🌐 English ⚖ 329 KB

Microdeletion of 17q22q23.2 encompassing

Microdeletion of 17q22q23.2 encompassing TBX2 and TBX4 in a patient with congenital microcephaly, thyroid duct cyst, sensorineural hearing loss, and pulmonary hypertension

✍ Manjunath Nimmakayalu; Heather Major; Val Sheffield; Donald H. Solomon; Richard 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 288 KB

## Abstract Microdeletions of the long arm of chromosome 17 are being reported with increasing frequency. Deletions of 17q22q23.2 may represent a genetically recognizable phenotype although its spectrum of genomic abnormalities, clinical manifestations, and critical regions are not fully delineated