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Ophthalmological findings in a case of 11 q deletion syndrome



Ophthalmological findings in a case of 11 q deletion syndrome



Klinische Monatsblaetter fuer Augenheilkunde 190(6): 524-526



A 5-year-old boy with deletion of the long arm of chromosome 11 presented with trigonocephaly, bilateral ptosis, epicanthus, antimongoloid lid axes, and bilateral iris coloboma. In order to avoid complication by a torticollis a Guyton-Friedenwald fadenoperation was performed. In 1981 Grosse et al. listed among the pediatric symptoms retarded development, ventricular septum defect, mitral stenosis, and skeletal and urogenital anomalies.

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Accession: 006036344

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