Results 51 to 60 of about 240,665 (151)

Congenital dacryocystocele: Retrospective evaluation of clinical features and treatment outcomes

, 2019
Amaç: Doğumsal dakriyosistoselli hastaların klinik özellikleri ve tedavi sonuçlarını gözden geçirmek. Gereç ve Yöntem: Ocak 1999 - Ağustos 2018 arasında tedavi edilen doğumsal dakriyosistoselli hastaların tıbbi kayıtları gözden geçirildi.
Efe, Ayşe Çetin
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Bilateral congenital dacryocystocele-A case report [PDF]

Biomedical Research, 2018
Congenital dacryocystocele is a rare congenital anomaly of the lacrimal drainage system (0.02% of newborns), which refers to the cystic dilatation of the lacrimal sac and nasolacrimal duct. In most cases the pathology is unilateral with female predominance.
Nevyana Veleva, Violeta Chernodrinska, Ognyan Mladenov   +2 more
openaire   +1 more source

Management of congenital dacryocystocele: report of 3 clinical cases

B-ENT, 2016
Management of congenital dacryocystocele: report of 3 clinical cases. This case study describes three newborns referred to our oto-laryngologic service for investigating and treating a cystic dilatation of the lacrimal duct.
F. Rogister, Y. Goffart, J. Daele
doaj   +2 more sources

Clinic‐Based Transnasal Marsupialization for the Treatment of Congenital Dacryocystocele

Objective To evaluate the feasibility and outcomes of endoscopic intranasal marsupialization as treatment for congenital dacryocystocele, performed under topical anesthesia in a clinical setting.
Rosanne Superstein, Erika Mercier, Annie Lapointe, Camille Caron, Charlotte Lussier   +4 more
core   +1 more source

A review of congenital heart block [PDF]

, 2003
Congenital heart block is a rare disorder. It has an incidence of about 1 in 22,000 live births. It may be associated with high mortality and morbidity.
Glickstein, J., Buyon, Jill P., Friedman, Deborah M., Duncanson, L.J.   +3 more
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The association between the congenital heart diseases and congenital anomalies of the kidney and the urinary tract in nonsyndromic children

, 2021
Several congenital heart diseases (CHD) are present in children with congenital anomalies of the kidney and the urinary tract (CAKUT) in syndromic or nonsyndromic patterns.
Muhammet İrfan Dönmez, Hayrullah Alp, KeleŞ Alp, Esma, Ahmet Midhat Elmacı, Dönmez, Muhammet İrfan, Alp, Hayrullah, Elmacı, Ahmet Midhat, Esma Keleş Alp   +7 more
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Consanguinity and the risk of congenital heart disease [PDF]

, 2012
Consanguineous unions have been associated with an increased susceptibility to various forms of inherited disease. Although consanguinity is known to contribute to recessive diseases, the potential role of consanguinity in certain common birth defects is
Hudgins, L., Shieh, J.T.C., Bittles, A.H.   +2 more
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Passive immunization during pregnancy for congenital cytomegalovirus infection

, 2005
BACKGROUND: Currently, there is no effective intervention for a primary cytomegalovirus (CMV) infection during pregnancy. METHODS: We studied pregnant women with a primary CMV infection.
Giuseppe Gentile, Congenital Cytomegalovirus Collaborating Group, Al M. Best, Giovanni Nigro, Stuart P. Adler, Renato La Torre   +5 more
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Preserved Statistical Learning of Tonal and Linguistic Material in Congenital Amusia [PDF]

, 2011
Congenital amusia is a lifelong disorder whereby individuals have pervasive difficulties in perceiving and producing music. In contrast, typical individuals display a sophisticated understanding of musical structure, even in the absence of musical ...
Stewart, Lauren, Lauren Stewart, Omigie, Diana, Stewart, L., Diana eOmigie, Lauren eStewart, Stewart, L; id_orcid, Diana Omigie, Omigie, D., Omigie, D   +9 more
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Gamma-D crystallin gene (CRYGD) mutation causes autosomal dominant congenital cerulean cataracts [PDF]

, 2003
Congenital cataracts are a major cause of bilateral visual impairment in childhood. We mapped the gene responsible for autosomal congenital cerulean cataracts to chromosome 2q33-35 in a four generation family of Moroccan descent. The maximum lod score (7.
Basak, A, Hilal, L., Cherif Chefchaouni, M., Slingsby, Christine, Hajaji, Y, Basak, Ajit K., Arbogast, L., Abitbol, Marc, M, Nandrot, E., Cherif-Chefchaouni, M, Benazzouz, B, Boutayeb, S, Boutayeb, S., Berraho, A., Hilal, Latifa, Abitbol, M., Arbogast, Laurence, Hajaji, Y., Gribouval, O., Benazzouz, B., Abitbol, Marc,, Nandrot, Emeline, Gribouval, Olivier   +22 more
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