Archives of Ophthalmology · 1991 · 65 citations · 20 references
Life SciencesGeneticsMolecular GeneticsHuman GeneticsMedical GeneticsOcular GeneticsCongenital Eye AnomaliesCorneal DisordersGenetic DisordersMendelian DisordersCorneal Dystrophy GeneticsCorneal Dystrophy Inheritance PatternsCorneal Dystrophy Molecular GeneticsInherited Ocular DiseaseInherited Ocular DisordersX-linked Congenital Cataract
We studied the clinical appearance and inheritance in five families with X-linked megalocornea. Affected male subjects had corneal diameters between 13.0 and 16.5 mm. Arcus juvenilis, mosaic corneal dystrophy, and cataracts were found only in adult affected male subjects. No carrier female abnormality was identified. The gene locus for the X-linked form is in the region Xq12-q26. This is near the locus described for Aarskog (facial-digital-genital) syndrome, Xq12-13.
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Developmental Abnormalities of the Eye
Journal of the American Medical Association · 1938 · 468 citations
Megalocornea associated with multiple skeletal anomalies: a new genetic syndrome?
Y Frank, Micha N. Ziprkowski, A Romano et al. · PubMed · 1973 · 50 citations
Life Sciences, Anatomy, Genetics +14
Ocular manifestations of the Marfan syndrome.
RANDY ALLEN, B. R. Straatsma, Leonard Apt et al. · PubMed · 1967 · 46 citations
Medicine, Neurology, Ophthalmology +13