Nontraumatic bilateral inferior ectopia lentis. [PDF]
Grassi P, Ramkissoon Y.
europepmc +1 more source
A De Novo 13q21.33-q31.1 Interstitial Deletion in a Child With Megalocornea and Neurodevelopmental Delay: A Clinico-Genomic Correlation. [PDF]
Elmakhzen B +3 more
europepmc +1 more source
Comparison of Anterior Segment Abnormalities in Individuals With FOXC1 and PITX2 Variants. [PDF]
Prem Senthil M +8 more
europepmc +1 more source
Endoscopic third ventriculostomy for diencephalosynapsis-related hydrocephalus in MPDZ gene syndrome: a case report and review of the literature. [PDF]
Cavalheiro S +7 more
europepmc +1 more source
Atypical presentations of non-familial anterior megalophthalmos: a rare disease. [PDF]
Rao A, Dcruz RP.
europepmc +1 more source
Ocular findings associated with chromosome 22q11.2 duplication.
We describe the ocular features of the chromosome 22q11.2 duplication syndrome and provide ophthalmologic examination recommendations for affected patients. The medical records of 19 children with chromosome 22q11.2 duplication who had undergone complete
Wootton, Georgia +5 more
core
Primary congenital glaucoma: Spontaneous resolution
Premanand Chandran +3 more
doaj +1 more source
Clinical and Multimodal Imaging Features of Familial Exudative Vitreoretinopathy: The Genetic and Phenotypic Spectrum. [PDF]
Öğreden T, Muftuoglu IK, Erdoğan G.
europepmc +1 more source
A case of mosaic Goltz syndrome in a male baby: Where persistence pays off. [PDF]
Gillespie Y +5 more
europepmc +1 more source

