Literature DB >> 17351350

New clinical findings in the Richieri-Costa/Pereira type of acrofacial dysostosis.

Marcelo B Golbert1, Lucas O Dewes, Viviane R Philipsen, Rebeca S Wachholz, Caroline Deutschendorf, Júlio C L Leite.   

Abstract

The Richieri-Costa/Pereira form of acrofacial dysostosis is an autosomal-recessive condition characterized by short stature, Pierre-Robin sequence, preaxial and postaxial abnormalities in hands, congenital talipes, cleft mandible and malformations of the larynx. We report female infant presenting with severe micrognathia, a hypoplasic clavicle, median mandible cleft, bilateral hand abnormalities and talipes, laryngeal malformations, hip subluxation with acetabular dysplasia and mesomelic shortening of limbs. A few reported patients have clavicular hyploplasia but hip subluxation with acetabular dysplasia and mesomelic shortening of limbs have not been described.

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Year:  2007        PMID: 17351350     DOI: 10.1097/MCD.0b013e3280464ff6

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN: 0962-8827            Impact factor:   0.816


  2 in total

1.  EIF4A3 deficient human iPSCs and mouse models demonstrate neural crest defects that underlie Richieri-Costa-Pereira syndrome.

Authors:  Emily E Miller; Gerson S Kobayashi; Camila M Musso; Miranda Allen; Felipe A A Ishiy; Luiz Carlos de Caires; Ernesto Goulart; Karina Griesi-Oliveira; Roseli M Zechi-Ceide; Antonio Richieri-Costa; Debora R Bertola; Maria Rita Passos-Bueno; Debra L Silver
Journal:  Hum Mol Genet       Date:  2017-06-15       Impact factor: 6.150

2.  [Laryngeal malformations in the Richieri Costa and Pereira syndrome with airway obstruction].

Authors:  Patrícia Barcelos Ogando; Fábio Pires; Rita Carolina Pozzer Krummenauer; Marcus Vinícius Martins Collares; José Faibes Lubianca Neto
Journal:  Braz J Otorhinolaryngol       Date:  2011 Jan-Feb
  2 in total

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