Create issue ticket

17 Possible Causes for Delayed Eruption of Primary and Secondary Teeth, Glaucoma, Ichthyosis

  • Oculodentodigital Dysplasia

    A 14-year-old girl with typical oculodentodigital syndrome had been treated for chronic glaucoma for seven years.[ncbi.nlm.nih.gov] Dental conditions frequently seen with this condition include: delayed eruption of primary or secondary (permanent) teeth, crowded/misaligned teeth, and increased incidence[polkdentistry.com] Missense mutations in the GJB2 encoding connexin-26 cause the ectodermal dysplasia keratitis-ichthyosis-deafness syndrome . Am J Hum Genet 2002; 70 (5): 1341–1348. 14.[nature.com]

  • Congenital Ichthyosis

    J Glaucoma . 2016 Mar. 25 (3):e280-3. [Medline] . Scheers C, Andre J, Thompson C, Rebuffat E, Harag S, Kolivras A.[emedicine.medscape.com] Oral and dental findings reported in itchthyosis patients included gingivitis, periodontitis, enamel hypoplasia, high caries incidence, delayed primary and secondary eruption[ijpd.in] The various types of congenital ichthyosis are usually diagnosed at birth, based on the characteristic appearance of the newborn.[symptoma.com]

  • Ichthyosis

    Congenital cataracts, glaucoma and microphthalmia have been reported in several individuals.[disorders.eyes.arizona.edu] Oral and dental findings reported in itchthyosis patients included gingivitis, periodontitis, enamel hypoplasia, high caries incidence, delayed primary and secondary eruption[ijpd.in] There are 5 major types of IT: Ichthyosis vulgaris (the most common of the five), recessive X-linked ichthyosis, autosomal recessive congenital ichthyosis-1 (ARCI1), keratinopathic[symptoma.com]

  • Familial Congenital Nasolacrimal Duct Obstruction

    Developmental glaucomas 4. Congenital iris ectropion syndrome A. Primary congenital glaucoma (PCG) 5. Peters’ syndrome 1. Newborn primary congenital glaucoma 6.[entokey.com] Dental Children and young adults with DS are at risk for: Significant delay in eruption of both primary and secondary teeth Missing and/or malformed teeth Dental crowding[medicalhomeportal.org] Congenital ichthyosis is autosomal recessive and genetically heterogeneous. Mutations in the TGM1(14q12) gene account for majority of cases.[reviewofophthalmology.com]

  • Gingival Fibromatosis-Progressive Deafness Syndrome

    […] lentis-microspherophakia-stiff joints-short stature syndrome Glaucoma secondary to spherophakia/ectopia lentis and megalocornea Glaucoma-sleep apnea syndrome GLB1 deficiency[orpha.net] primary teeth eruption, failure of secondary teeth eruption, corneal dystrophy, aggressive behaviour [ 192 – 194 ].[ojrd.biomedcentral.com] […] skeletal anomalies Juvenile retinoschisis Deafness, epiphyseal dysplasia, short stature Angioma hereditary neurocutaneous Mucopolysaccharidosis type IIIC Macrozoospermia Ichthyosis[checkrare.com]

  • Bloch Sulzberger Syndrome

    […] authors present the pathological findings in the skin and eye in a young woman who required enucleation as a result of long-standing retinal detachment and closed-angle glaucoma[ncbi.nlm.nih.gov] These abnormalities include a delay in the eruption of primary teeth; abnormal contours of teeth, giving them a peg-like or cone-shaped appearance; or the congenital absence[rarediseases.org] 29 FabryAnderson Disease 265 Chapter 30 Adrenoleukodystrophy 273 Chapter 31 Kinky Hair Disease 284 Chapter 32 Incontinentia Pigmenti 293 Chapter 33 A Syndrome of Anosmia Ichthyosis[books.google.com]

  • X-Linked Mandibulofacial Dysostosis

    Cataracts and glaucoma require attention when present, of course.[disorders.eyes.arizona.edu] […] or completefailure of eruption of permanent teethHistology:Unerupted permanent teeth lack secondary cementumTreatment:No treatment; full-mouth extractions with denture construction[slideshare.net] ( 1 Files ) Disease name: Lamellar ichthyosis ICD 10: Q80.2 Synonyms: Autosomal recessive congenital ichthyosis, bathing-suit ichthyosis (limited to the trunk) Lowe syndrome[orphananesthesia.eu]

  • Congenital Non-Bullous Ichthyosiform Erythroderma ARCI 10

    METHODS: We present a case of NBCIE with glaucoma and dwarfism that presented to our outpatient department.[readbyqxmd.com] Oral and dental findings reported in itchthyosis patients included gingivitis, periodontitis, enamel hypoplasia, high caries incidence, delayed primary and secondary eruption[ijpd.in] The Blueprint Genetics ichthyosis panel covers classical genes associated with congenital ichthyosis, lamellar ichthyosis and multiple sulfatase deficiency.[blueprintgenetics.com]

  • Autosomal Recessive Congenital Ichthyosis Type 4

    J Glaucoma. 2016 Mar. 25 (3):e280-3. [Medline]. Scheers C, Andre J, Thompson C, Rebuffat E, Harag S, Kolivras A.[emedicine.medscape.com] Oral and dental findings reported in itchthyosis patients included gingivitis, periodontitis, enamel hypoplasia, high caries incidence, delayed primary and secondary eruption[ijpd.in] , the most severe form of congenital ichthyosis, is characterized by a thickening of the keratin layer in fetal skin.[flipper.diff.org]

  • Crane-Heise Syndrome

    Hodgkin lymphoma Globoid cell leukodystrophy hypotonia telangiectasia upper lip and dental roots XC Classical Hodgkin's lymphoma Globoid cell Mental retardation athetosis glaucoma[yumpu.com] (hyperdontia) in the primary and secondary dentition resulting in crowding and malocclusion, retention of deciduous teeth, delayed eruption of secondary dentition and failure[wiki.romse.org] Pombo Novo syndrome * Cat Eye syndrome * Cat Rodrigues syndrome * Cat Scratch Disease * Catamenial pneumothorax * Cataplexy * Cataract and cardiomyopathy * Cataract and congenital[medicalgeek.com]

Similar symptoms