Syndromic and nonsyndromic systemic associations of congenital lacrimal drainage anomalies: a major review

MJ Ali, F Paulsen - Ophthalmic Plastic & Reconstructive Surgery, 2017 - journals.lww.com
Purpose: To review and summarize the syndromic, nonsyndromic, and systemic
associations of congenital lacrimal drainage anomalies. Methods: The authors performed a …

Embryology of the lacrimal drainage system

MJ Ali, H Kakizaki - Principles and practice of lacrimal surgery, 2018 - Springer
The understanding of lacrimal embryology is very crucial to the understanding of lacrimal
anatomy and its subsequent clinical and surgical applications. In addition, numerous …

Congenital nasolacrimal duct obstructions

S Kamal, MJ Ali, V Gauba - Principles and practice of lacrimal surgery, 2018 - Springer
Congenital nasolacrimal duct obstruction (CNLDO) is a common cause of epiphora in
children. Management of CNLDO is principally guided by natural history of disease and high …

[HTML][HTML] Comparative proteomics of mouse tears and saliva: evidence from large protein families for functional adaptation

RC Karn, CM Laukaitis - Proteomes, 2015 - mdpi.com
We produced a tear proteome of the genome mouse, C57BL/6, that contained 139 different
protein identifications: 110 from a two-dimensional (2D) gel with subsequent trypsin …

Ocular manifestations in Koolen–de Vries syndrome: an international study

D Shalev, DA Koolen, BBA de Vries… - Canadian Journal of …, 2023 - Elsevier
Abstract Objectives Koolen–de Vries Syndrome (KdVS) is a rare multisystem
neurodevelopmental disorder. Ocular manifestations, including strabismus, ptosis, and …

Lacrimal Obstruction in Craniosynostosis: Anatomical and Genetic Risk Factors

D Landau-Prat, JA Taylor, CL Kalmar… - Ophthalmic Plastic & …, 2024 - journals.lww.com
Purpose: To investigate whether patients with craniosynostosis exhibit higher rates of
nasolacrimal duct obstruction (NLDO) and to explore potential risk factors. Methods …

New pathogenic variant in the FGF10 gene in the agenesis of lacrimal and salivary gland syndrome: Ophthalmological and genetic study

MJ Rodrigo, M Idoipe, S Izquierdo, M Satue… - Ophthalmic …, 2018 - Taylor & Francis
Aplasia/agenesis of lacrimal and salivary glands is a rare congenital defect that has been
associated with disturbances in fibroblast growth factor 10 (FGF10). It can present with …

Angeborene Fehlbildungen der ableitenden Tränenwege

J Heichel, LM Heindl, HG Struck - Klinische Monatsblätter für …, 2022 - thieme-connect.com
Congenital dacryostenosis is the most common reason for ophthalmic consultation in
childhood. It is most often caused by persisting of Hasnerʼs membrane. However …

[HTML][HTML] Malformation of tear ducts underlies the epiphora and precocious eyelid opening in prickle 1 mutant mice: genetic implications for tear duct genesis

J Ru, D Guo, J Fan, J Zhang, R Ju… - … & Visual Science, 2020 - iovs.arvojournals.org
Purpose: Obstruction of the tear drainage causes a range of ocular surface disorders.
Hitherto, the genetics of tear duct development and obstruction has been scarcely explored …

[HTML][HTML] Isolated Congenital Lacrimal Gland Agenesis

GB Bilgin, C Bilgin, A Orscelik, B Musmar… - Cureus, 2024 - ncbi.nlm.nih.gov
Congenital alacrima is an uncommon condition marked by a lack of tear production that is
present from birth. This condition often occurs in conjunction with various syndromes but can …