Pierre Robin syndrome: a case report.

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dc.contributor.authorGupta, Richa
dc.contributor.authorPatel, Meena
dc.contributor.authorBajaj, Naresh
dc.date.accessioned2015-12-02T09:17:34Z
dc.date.available2015-12-02T09:17:34Z
dc.date.issued2015-11
dc.description.abstractPierre Robin syndrome is characterized by micrognathia, glossoptosis and palatal malformation. We report a case of a 6 day neonate who presented with complaints of feeding and respiratory difficulty and was later diagnosed as case of Pierre Robin syndrome.en_US
dc.identifier.citationGupta Richa, Patel Meena, Bajaj Naresh. Pierre Robin syndrome: a case report. International Journal of Research in Medical Sciences. 2015 Nov; 3(11): 3432-3434.en_US
dc.identifier.issn2320-6071
dc.identifier.issn2320-6012
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/166858
dc.language.isoenen_US
dc.source.urihttps://www.msjonline.org/?mno=202012en_US
dc.subjectCleft palateen_US
dc.subjectMicrognathiaen_US
dc.subjectGlossoptosisen_US
dc.subjectPierre Robin syndromeen_US
dc.titlePierre Robin syndrome: a case report.en_US
dc.typeArticleen_US
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