Create issue ticket

16 Possible Causes for Glaucoma, Mild Maxillary Prognathism

  • Rieger Syndrome

    Approximately 75% of ARS patients with FOXC1 mutations develop earlier-onset glaucoma.[ncbi.nlm.nih.gov] Facies: - Maxillary hypoplasia - Mild prognathism ... Teeth: - Microdontia - Hypodontia - Cone - shaped teeth ... Ear: - Abnormal ear ... Abdomen: - Umbilical hernia ...[ibis-birthdefects.org] They include mild dysmorphism (hypertelorism, broad flat nose, maxillary hypoplasia, and mild prognathism), dental anomalies (microdontia, hypodontia, anodontia, oligodontia[glaucomatoday.com]

  • Peters Anomaly

    CONCLUSIONS: Glaucoma surgery, combined with medical therapy, may result in adequate, long-term IOP control in 32% of eyes with glaucoma associated with Peters' anomaly.[ncbi.nlm.nih.gov] They include mild dysmorphism (hypertelorism, broad flat nose, maxillary hypoplasia, and mild prognathism), dental anomalies (microdontia, hypodontia, anodontia, oligodontia[glaucomatoday.com] KEYWORDS: 22q11.2 deletion syndrome; CYP1B1; congenital glaucoma; peters anomaly[ncbi.nlm.nih.gov]

  • Axenfeld-Rieger Syndrome Type 3

    In pedigrees 1,2, and 4, younger generations had iris hypoplasia with severe early-onset glaucoma, whereas their parents had posterior embryotoxon without glaucoma.[journals.lww.com] They include mild dysmorphism (hypertelorism, broad flat nose, maxillary hypoplasia, and mild prognathism), dental anomalies (microdontia, hypodontia, anodontia, oligodontia[glaucomatoday.com] Exposure to topical apraclonidine in children with glaucoma. J Glaucoma. 2009;18(5):395-8. 25.0 25.1 25.2 Beck AD. Diagnosis and management of pediatric glaucoma.[eyewiki.aao.org]

  • Craniosynostosis Type 3

    […] pustular psoriasis Genetic hyperparathyroidism Genetic neuromuscular disease Genetic peripheral neuropathy Genetic syndromic Pierre Robin syndrome Giant axonal neuropathy Glaucoma[sanfordresearch.org] Note maxillary hypoplasia, ocular proptosis with mild relative prognathism. (From Renier et al. 2000) syndrome is genetically heterogeneous.[rrnursingschool.biz] Ophthalmological disorders Most commonly: Cataracts Refractive errors Strabismus Nystagmus Congenital glaucoma Keratoconus Gastrointestinal disorders Oesophageal atresia or[patient.info]

  • Isolated Trigonocephaly

    Glaucoma With Crouzon Syndrome. J Glaucoma. 2018 Jun;27(6):e110-e112. doi: 10.1097/IJG.0000000000000946.[eyewiki.aao.org] Note maxillary hypoplasia, ocular proptosis with mild relative prognathism. (From Renier et al. 2000) syndrome is genetically heterogeneous.[rrnursingschool.biz] […] two were excluded because of syndromic diagnosis (trisomy 18 and Dandy-Walker syndrome), three were excluded because of a history of primary ocular disorder (congenital glaucoma[cappskids.org]

  • Peters Anomaly - Cataract Syndrome

    […] classifications and outcomes.Coherently correlates with authoritative consensus documents on key areas of glaucoma, drawn up by the world-wide specialists of the World Glaucoma[books.google.de] They include mild dysmorphism (hypertelorism, broad flat nose, maxillary hypoplasia, and mild prognathism), dental anomalies (microdontia, hypodontia, anodontia, oligodontia[glaucomatoday.com] glaucoma patients and greater public awareness of glaucoma.[pgcfa.org]

  • Congenital Ectropion Uveae

    We report three cases with CEU of which two already developed glaucoma. All patients with CEU should be carefully examined periodically to detect glaucoma.[ncbi.nlm.nih.gov] They include mild dysmorphism (hypertelorism, broad flat nose, maxillary hypoplasia, and mild prognathism), dental anomalies (microdontia, hypodontia, anodontia, oligodontia[glaucomatoday.com] If the patient is followed glaucoma will always be found to be present.[ncbi.nlm.nih.gov]

  • Familial Scaphocephaly Syndrome

    Glaucoma With Crouzon Syndrome. J Glaucoma. 2018 Jun;27(6):e110-e112. doi: 10.1097/IJG.0000000000000946.[eyewiki.aao.org] Note maxillary hypoplasia, ocular proptosis with mild relative prognathism. (From Renier et al. 2000) syndrome is genetically heterogeneous.[rrnursingschool.biz] Congenital glaucoma secondary to closed angles and FGFR2-related anterior segment dysgenesis has been reported [11].[eyewiki.aao.org]

  • De Hauwere Syndrome

    Quantitative correlation of nerve fiber loss and visual field defect in glaucoma, ischemic neuropathy, papilledema, and toxic neuropathy. ‎[books.google.es] Nonocular features included characteristic facies (maxillary hypoplasia, short philtrum, and protruding lower lip of mild prognathism), dental anomalies (microdontia, hypodontia[genome.jp] There are no reports of glaucoma but this may be biased by the small number of patients reported. Hypertelorism, prominent eyes and strabismus have been described.[disorders.eyes.arizona.edu]

  • Baller-Gerold Syndrome

    Fibrochondrogenesis Floating Harbor syndrome Fragile X Syndrome Freeman-Sheldon Syndrome Fryns syndrome Fucosidosis Glaucoma - Congenital Glutaric Aciduria Type I and II Glycogen[de.slideshare.net] Note maxillary hypoplasia, ocular proptosis with mild relative prognathism. (From Renier et al. 2000) syndrome is genetically heterogeneous.[rrnursingschool.biz] Prader-Willi Syndrome PRICKLE1-Related Progressive Myoclonus Epilepsy with Ataxia Primary Autosomal Recessive Microcephaly Primary Ciliary Dyskinesia Primary Congenital Glaucoma[genetests.org]

Further symptoms

Similar symptoms