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Ring chromosome 22: a case report.

C Severien·S Felix·K Bartholomé
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Abstract

A three year old girl with ring chromosome 22 is described. The clinical findings include epicanthus, flat nasal bridge, hypertelorism, long eye-lashes, lymphoedema, hypoplastic toe nails, hydrocephalus and muscular hypotonia. Speech and language development is delayed. At three years the child begins to walk.

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Abnormalities, MultipleChild, PreschoolChromosome AberrationsChromosome DisordersChromosomes, Human, Pair 22Developmental DisabilitiesFacial BonesFemaleHumansHypertelorismInfant, NewbornKaryotypingMuscle HypotoniaRing ChromosomesCase ReportsJournal Article

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C Severien, S Felix, K Bartholomé. Ring chromosome 22: a case report.. https://doi.org/10.1055/s-2007-1025476

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