Results 1 to 10 of about 46,879 (178)
Pierre Robin sequence and keratoconus, a rare association [PDF]
Iberoamerican Journal of Medicine, 2022 Pierre Robin sequence (PRS) is an inherited disorder that affects one in between 8,500 and 14,000 people and is characterized by a triad of clinical signs. These include micrognathia, glossoptosis and obstruction of the upper airway, typically associated
Jorge Hernández-Cerdá +2 more
doaj +2 more sources
SEMI-AUTOMATIC VOLUMETRIC SEGMENTATION OF THE UPPER AIRWAYS IN PATIENTS WITH PIERRE ROBIN SEQUENCE [PDF]
, 2014 Pierre Robin malformation is a rare craniofacial dysmorphism whose pathogenesis is multifactorial. Although there is some agreement in non-invasive treatment in less severe cases, the dispute is still open on cases with severe respiratory impairment.
Gagliardo, C. +7 more
core +3 more sources
Brazilian Journal of Otorhinolaryngology, 2022 Introduction: Obstructive sleep apnea is highly prevalent in non-syndromic Pierre Robin sequence patients. Studies have found a probable relationship between obstructive sleep apnea and nasal obstruction and between obstructive sleep apnea and enuresis ...
Fábio Luiz Banhara +4 more
doaj +2 more sources
Cleft palate in Pierre Robin sequence [PDF]
E3S Web of Conferences, 2021 Pierre Robin’s sequence PRS is a congenital malformative sequence with a retrognathism, a glossoptosis and an upper respiratory obstruction with an associated cleft palate. This malformative association can be disabling for both the child and his parents,
Oubejja Houda +5 more
doaj +1 more source
Frontiers in Pediatrics, 2021 Objectives: Cyproheptadine is a first-generation H1-antihistamine drug first that was distributed in the 1960s. While its orexigenic effect was observed early, cyproheptadine is not yet authorized for this indication in all countries today.
Valérie Bertrand +10 more
doaj +1 more source
Anorectal Malformation: An Atypical Association of Pierre Robin Sequence [PDF]
Pediatric Sciences Journal, 2022 Isolated Pierre Robin sequence (PRS) is characterized by underdeveloped jaw, backward displacement of the tongue and upper airway obstruction with or without cleft palate or be part of a known syndrome as VACTREL or CHARGE, or be associated with other ...
Manal M. Farouk +2 more
doaj +1 more source
Clinical Case Reports, 2023 Key Clinical Message Femoral hypoplasia‐unusual facies syndrome is a rare condition of unknown etiology. The phenotype consists of significant femoral hypoplasia with characteristic facial malformations that often overlap with findings seen in patients ...
Lauren M. Partyka
doaj +1 more source
Cleft palate in Pierre Robin syndrome: A Review of 7 cases
Advances in Oral and Maxillofacial Surgery, 2023 Introduction: Pierre Robin syndrome is a malformative sequence associating retrognathism, glossoptosis and a median cleft palate which is usually large. This poses the problem of its therapeutic management.
A.D.C. Opango +5 more
doaj +1 more source
Best practices for the diagnosis and evaluation of infants with robin sequence:a clinical consensus report [PDF]
, 2016 Importance: Robin sequence (RS) is a congenital condition characterized by micrognathia, glossoptosis, and upper airway obstruction. Currently, no consensus exists regarding the diagnosis and evaluation of children with RS.
Abadie, Veronique +23 more
core +6 more sources
Brazilian Journal of Otorhinolaryngology, 2009 Asequência de Pierre Robin é caracterizada por micrognatia, glossoptose e obstrução das vias aéreas superiores. A gravidade dos sintomas é muito variável, o que torna o tratamento destes pacientes um desafio.
Carlos Diógenes Pinheiro Neto +4 more
doaj +1 more source