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


Autoria(s): Rossi, N. F.; Gatto, A. R.; Cola, P. C.; Souza, D. H.; Moretti-Ferreira, D.; Giacheti, C. M.
Contribuinte(s)

Universidade Estadual Paulista (UNESP)

Data(s)

20/05/2014

20/05/2014

01/01/2009

Resumo

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.

Formato

1133-1138

Identificador

http://dx.doi.org/10.4238/vol8-3gmr621

Genetics and Molecular Research. Ribeirao Preto: Funpec-editora, v. 8, n. 3, p. 1133-1138, 2009.

1676-5680

http://hdl.handle.net/11449/12505

10.4238/vol8-3gmr621

WOS:000272050000023

WOS000272050000023.pdf

Idioma(s)

eng

Publicador

Funpec-editora

Relação

Genetics and Molecular Research

Direitos

openAccess

Palavras-Chave #Deglutition evaluation #Language evaluation #Deglutition disorders #Language delay #Partial trisomy 9p
Tipo

info:eu-repo/semantics/article