Ring D Chromosome 131h72b 131h72b 131h72b 131h72b 131h72b 131h72b
General: Variant of the chromosome 13 deletion syndrome; ring chromosomes.
Ocular: Hypertelorism; epicanthal folds; ptosis; microphthalmos; uveal colobomas; abnormal palpebral fissure; strabismus; retinoblastoma.
Clinical: Aplasia of thumbs; mental and physical retardation; trigonocephaly; malrotation of ear; micrognathia; hypoplastic nipple; widely spaced first and second toes.
Collins JF. Handbook of Clinical Ophthalmology. New York: Masson, 1982.
Magalini SI, Scrascia E. Dictionary of Medical Syndromes, 2nd ed. Philadelphia: JB Lippincott, 1981:711.
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