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1,104 Possible Causes for Pierre Robin Syndrome

  • Congenital Mandibular Hypoplasia

    Pierre Robin syndrome. Preoperative appearance. Pierre Robin syndrome. Preoperative appearance.[emedicine.medscape.com] Pierre Robin syndrome and mandibulofacial dysostosis versus isolated mandibular hypoplasia Pierre Robin syndrome and MFD syndromes are both defects of the branchial arches[jofs.in] Pierre Robin syndrome : micrognathia, glossoptosis, and cleft palate Treacher Collins syndrome : hypoplasia of facial bones, especially malar and mandibular bones, malformation[radiopaedia.org]

  • Nager Syndrome

    The present patient had typical findings of Nager syndrome and Pierre Robin sequence.[ncbi.nlm.nih.gov] Synonyms: Pierre Robin syndrome (PRS), Pierre Robin anomaly/anomalad, Pierre Robin malformation (PRM) complex, Robin sequence, Robin complex Related conditions - these may[patient.info] Doctors told Emi and Andrew that she may have Pierre Robin syndrome, where a smaller than normal lower jaw causes breathing problems.[gosh.nhs.uk]

  • Pierre Robin Syndrome

    […] enwiki Pierre Robin syndrome eswiki Síndrome de Pierre Robin euwiki Robinen sindromea frwiki Syndrome de Pierre Robin itwiki Sindrome di Pierre Robin kkwiki Робен синдромы[wikidata.org] Pierre Robin syndrome may also occur as one of the features of other syndromes or defects.[symptoma.com] These hand abnormalities have not been previously emphasized in patients with the Pierre Robin syndrome.[ncbi.nlm.nih.gov]

  • Micrognathism

    The diagnosis of Pierre-Robin syndrome was made postnatally. The possible differential diagnoses and the main complications of retrognathism are reviewed.[link.springer.com] Juvenile idiopathic arthritis Marfan syndrome Noonan syndrome Pierre Robin syndrome Prader–Willi syndrome Progeria Silver–Russell syndrome Seckel syndrome Smith–Lemli–Opitz[en.wikipedia.org] Pierre Robin Syndrome Pierre Robin syndrome causes your baby’s jaw to form slowly in the womb, which results in a very small lower jaw.[healthline.com]

  • Stickler Syndrome

    The most frequent diagnosis in patients with syndromic Pierre Robin sequence is Stickler syndrome, which may be complicated by congenital high myopia and substantial risk[ncbi.nlm.nih.gov] An image depicting Pierre Robin syndrome can be seen below. A 5-month-old baby with Pierre Robin sequence and severe micrognathia.[emedicine.medscape.com] Birth Defects 10: 432–437 Google Scholar Smith WK (1969) Pierre Robin syndrome in brothers.[link.springer.com]

  • High Myopia-Sensorineural Deafness Syndrome

    Orofacial Structure The most severe problem associated with Stickler syndrome is Pierre Robin syndrome.[wikidoc.org] Orofacial Structure [ edit ] The most severe problem associated with Stickler syndrome is Pierre Robin syndrome.[en.wikipedia.org] MIM Entry: 277610 Title: #277610 WEISSENBACHER-ZWEYMULLER SYNDROME; WZS ;;PIERRE ROBIN SYNDROME WITH FETAL CHONDRODYSPLASIA Text: A number sign (#) is used with this entry[genome.jp]

  • Cerebro-Costo-Mandibular Syndrome

    This rare dysmorphic disorder (only 51 cases have been reported to date) mainly associates defective costal development with features of the Pierre-Robin syndrome.[ncbi.nlm.nih.gov] Research of Cerebro-costo-mandibular Syndrome has been linked to Micrognathism, Pierre Robin Syndrome, Cleft Palate, Congenital Abnormality, Dysplasia.[novusbio.com] We present an antenatal ultrasonographic diagnosis of the cerebro-costo-mandibular syndrome.[ncbi.nlm.nih.gov]

  • Prata-Libéral-Gonçalves Syndrome

    Robin nanism polydactyly Pierre Robin, sequence of Pierre Robin sequence of faciodigitale anomaly Pierre Robin syndrome chondrodysplasy Pierre Robin, syndrome of Pierre Robin[wikipedia.qwika.com] Pierre Robin sequence faciodigital anomaly Pierre Robin syndrome fetal chondrodysplasia Pierre Robin syndrome hyperphalangy clinodactyly Pierre Robin syndrome skeletal dysplasia[mindmappedia.com] […] ataxia Pierre Robin sequence congenital heart defect talipes Pierre Robin sequence faciodigital anomaly Pierre Robin syndrome fetal chondrodysplasia Pierre Robin syndrome[bioreference.net]

  • Stickler Syndrome Type 5

    An image depicting Pierre Robin syndrome can be seen below. A 5-month-old baby with Pierre Robin sequence and severe micrognathia.[emedicine.medscape.com] A particular group of physical features, called the Pierre Robin sequence, is common in children with Stickler syndrome.[en.wikipedia.org] In 1926, Pierre Robin published the case of an infant with the complete syndrome.[emedicine.medscape.com]

  • Pfeiffer-Palm-Teller Syndrome

    Robin nanism polydactyly Pierre Robin, sequence of Pierre Robin sequence of faciodigitale anomaly Pierre Robin syndrome chondrodysplasy Pierre Robin, syndrome of Pierre Robin[wikipedia.qwika.com] […] ataxia Pierre Robin sequence congenital heart defect talipes Pierre Robin sequence faciodigital anomaly Pierre Robin syndrome fetal chondrodysplasia Pierre Robin syndrome[bioreference.net] Pierre Robin syndrome fetal chondrodysplasia[?] Pierre Robin syndrome hyperphalangy clinodactyly[?] Pierre Robin syndrome skeletal dysplasia polydactyly[?][encyclopedia.kids.net.au]

Further symptoms