Literature DB >> 19866432

Oropharyngeal dysphagia and language delay in partial trisomy 9p: case report.

N F Rossi1, A R Gatto, P C Cola, D H Souza, D Moretti-Ferreira, C M Giacheti.   

Abstract

The phenotype of partial trisomy 9p includes global developmental delay, microcephaly, bulbous nose, downturned oral commissures, malformed ears, hypotonia, and severe cognitive and language disorders. We present a case report and a comparative review of clinical findings on this condition, focusing on speech-language development, cognitive abilities and swallowing evaluation. We suggest that oropharyngeal dysphagia should be further investigated, considering that pulmonary and nutritional disorders affect the survival and quality of life of the patient. As far as we know, this is the first study of a patient with partial trisomy 9p described with oropharyngeal dysphagia.

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Year:  2009        PMID: 19866432     DOI: 10.4238/vol8-3gmr621

Source DB:  PubMed          Journal:  Genet Mol Res        ISSN: 1676-5680


  1 in total

1.  Partial Trisomy 9p(p22→pter) from a Maternal Translocation 4q35 and 9p22.

Authors:  F Mahjoubi; F Nasiri; R Torabi
Journal:  Balkan J Med Genet       Date:  2011-06       Impact factor: 0.519

  1 in total

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