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658 Possible Causes for Maxillary Hypoplasia

  • Nasopalpebral Lipoma - Coloboma - Telecanthus Syndrome

    hypoplasia.[esanatos.com] […] malformation entity with autosomal dominant inheritance characterized by the combination of nasopalpebral lipoma, colobomas in upper and lower eyelids, telecanthus, and maxillary[jhu.pure.elsevier.com] […] extremely uncommon autosomal dominant condition characterized by congenital upper eyelid and nasopalpebral lipomas, colobomata of upper and lower eyelids, telecanthus, and maxillary[abdn.pure.elsevier.com]

  • Axenfeld Syndrome

    Systemic anomalies are associated, including dental hypoplasia, failure of involution of periumbilical skin, and maxillary hypoplasia (Alkemade, 1969).[ncbi.nlm.nih.gov] These patients might have a difficult airway due to facial anomalies, brachycephaly and maxillary hypoplasia.[aeronline.org] Examination revealed maxillary hypoplasia, thin upper lip, protruding lower lip and flattening of the mid face [Figure 1] and [Figure 2] .[aeronline.org]

  • Crouzon Syndrome

    INTRODUCTION: Crouzon syndrome is an autosomal dominant genetic disease characterized by bicoronal craniosynostosis, exorbitism with hypertelorism, and maxillary hypoplasia[ncbi.nlm.nih.gov] Crouzon syndrome is a craniostenotic craniofacial malformation associated with premature closure of selective calvarial sutures, exophthalmos, maxillary hypoplasia, and a[ncbi.nlm.nih.gov] Orofacial manifestations of this disease include maxillary hypoplasia, external nasal deformity, and prognathism.[ncbi.nlm.nih.gov]

  • Rieger Syndrome

    Synonym(s): iridocorneal mesodermal dysgenesis Rieger syndrome - Rieger anomaly combined with hypodontia or anodontia and maxillary hypoplasia.[medical-dictionary.thefreedictionary.com] At presentation, typical components of ARS could be found in both patients, including iris anomaly, maxillary hypoplasia, hypodontia, and umbilical skin fold.[ncbi.nlm.nih.gov] Additional features include aniridia, maxillary hypoplasia, hypodontia, anal stenosis, redundant periumbilical skin.[uniprot.org]

  • Non-Eruption of Teeth-Maxillary Hypoplasia-Genu Valgum Syndrome

    Diagnosis - Teeth noneruption of with maxillary hypoplasia and genu valgum Not supplied.[checkorphan.org] Diseases related to Teeth, Noneruption of, with Maxillary Hypoplasia and Genu Valgum via text searches within MalaCards or GeneCards Suite gene sharing: Symptoms via clinical[malacards.org] Resources - Teeth noneruption of with maxillary hypoplasia and genu valgum Not supplied.[checkorphan.org]

  • Axenfeld-Rieger Syndrome Type 3

    Diagnosis is best made by ruling out mutations in PITX1 and FOXC1 although it is claimed that maxillary hypoplasia and umbilical defects are less common in type 2.[disorders.eyes.arizona.edu] Systemic anomalies include craniofacial dysmorophisms such as hypertelorism, telecanthus, maxillary hypoplasia, and a broad, flat nasal bridge.[webeye.ophth.uiowa.edu] Anomalies include anterior segment dysgenesis of the eye, dental anomalies, maxillary hypoplasia, periumbilical anomalies, and congenital heart defects.[karger.com]

  • Tunglang-Savage-Bellman Syndrome

    hypoplasia and genu valgum Tel Hashomer camptodactyly syndrome Telangiectasia ataxia variant V1 Telangiectasia, hereditary hemorrhagic Telangiectasia Telecanthus hypertelorism[wikidoc.org] Taybi syndrome Tay-Sachs disease T-cell lymphoma Te-Th Teebi Kaurah syndrome Teebi Naguib Alawadi syndrome Teebi Shaltout syndrome Teebi syndrome Teeth noneruption of with maxillary[bioreference.net] […] syndrome Tay–Sachs disease T-cell lymphoma Te Tee–Ten Teebi–Kaurah syndrome Teebi–Naguib–Alawadi syndrome Teebi–Shaltout syndrome Teebi syndrome Teeth noneruption of with maxillary[ipfs.io]

  • Apert Syndrome

    A concave profile and a skeletal Class III jaw-base relationship caused by severe maxillary hypoplasia were seen in all patients.[ncbi.nlm.nih.gov] Abstract Apert syndrome is characterised by craniosynostosis, associated with maxillary hypoplasia, symmetrical syndactyly of the hands and feet, and other systemic malformations[ncbi.nlm.nih.gov] Abstract Apert syndrome is a congenital condition characterized by craniosynostosis, syndactyly, and maxillary hypoplasia.[ncbi.nlm.nih.gov]

  • Aarskog Syndrome

    Primary criteria include: short stature, hypertelorism, short nose with anteverted nares, maxillary hypoplasia, a crease below the lower lip, mild interdigital webbing with[ncbi.nlm.nih.gov] hypoplasia, hypodontia, retarded dental eruption, orthodontic problems 3.[web.archive.org] hypoplasia and transverse crease below the lower lip.[orpha.net]

  • Axenfeld Anomaly

    Diagnosis is best made by ruling out mutations in PITX1 and FOXC1 although it is claimed that maxillary hypoplasia and umbilical defects are less common in type 2.[disorders.eyes.arizona.edu] The patient was noted to have maxillary hypoplasia and mild mental retardation.[healio.com] These patients might have a difficult airway due to facial anomalies, brachycephaly and maxillary hypoplasia.[aeronline.org]

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