Mesodermal Dysgenesis (Anterior Chamber Dysgenesis; Dysembryogenesis; Anterior Segment Ocular Dysgenesis Syndrome) 818i81i 818i81i 818i81i 818i81i 818i81i 818i81i 7
General: Mesodermal abnormalities, including oculocutaneous albinism; autosomal dominant.
Ocular: Capsular cataracts; external ophthalmoplegia; anterior chamber cleavage syndrome; atrophy of iris; ectropion; flat cornea; coloboma of iris and choroid; posterior embryotoxon; Axenfeld anomaly; Rieger anomaly; Peters anomaly; keratoconus; microphthalmos.
Clinical: None.
Ferrell RE, et al. Anterior segment mesenchymal dysgenesis; probable linkage to the MNS blood group on chromosome 4. Am J Hum Genet 1982; 24:245-249.
Lubin JR. Oculocutaneous albinism associated with corneal mesodermal dysgenesis. Am J Ophthalmol 1981; 91:347-350.
Lubin JR. Oculocutaneous albinism and corneal mesodermal dysgenesis. Am J Ophthalmol 1981; 92:587.
Ghose S, et al. Microphthalmos and anterior segment dysgenesis in a family. Ophthalmic Paediatr Genet 1991; 12:177-l82.
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