COMPLEX CHROMOSOME REARRANGEMENT IN A CHILD WITH MICROCEPHALY, DYSMORPHIC FACIAL FEATURES AND MOSAICISM FOR A TERMINAL DELETION DEL(18)(Q21.32-QTER) INVESTIGATED BY FISH AND ARRAY-CGH: CASE REPORT

Complex chromosome rearrangement in a child with microcephaly, dysmorphic facial features and mosaicism for a terminal deletion del(18)(q21.32-qter) investigated by FISH and array-CGH: Case report

Abstract We report on a 7 years and 4 months old Greek boy with mild microcephaly and dysmorphic facial features.He was click here a sociable child with maxillary hypoplasia, epicanthal folds, upslanting palpebral fissures with long eyelashes, and hypertelorism.His ears were prominent and dysmorphic, he had a long philtrum and a high arched palate.

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