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15 Possible Causes for Delayed Eruption of Primary and Secondary Teeth, Glaucoma, Xeroderma

  • Ichthyosis

    Congenital cataracts, glaucoma and microphthalmia have been reported in several individuals.[] Ichthyosis, also called fish-skin disease, or xeroderma, a hereditary condition involving dryness and scaliness of the skin brought about by excessive growth of the horny[] Oral and dental findings reported in itchthyosis patients included gingivitis, periodontitis, enamel hypoplasia, high caries incidence, delayed primary and secondary eruption[]

  • 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.[] […] syndrome Maternal PKU fetal effect Meckel-Gruber syndrome Melnick-Fraser syndrome Menkes kinky-hair syndrome Mental retardation, dwarfism, and gonadal hypoplasia due to xeroderma[] 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[]

  • SHORT Syndrome

    We describe a child who had congenital glaucoma and SHORT syndrome. Report of a Case.[] The syndrome is sometimes differentiated as type 1 or a (onset at age 2 years or later), type 2 or b (named later comfak, q.v.), and type 3 or c (considered as a part of xeroderma[] The eruption of primary and secondary teeth may be delayed for up to 1.3 years in children with growth hormone deficiency, up to 1.5 years in children with CDGP and more than[]

  • 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[] Convert to ICD-10-CM : 757.33 converts approximately to: 2015/16 ICD-10-CM Q82.1 Xeroderma pigmentosum Or: 2015/16 ICD-10-CM Q82.2 Mastocytosis Approximate Synonyms Anomaly[] 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[]

  • 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[] Pigmentosum Type 7 2 Xeroderma Pigmentosum, Complementation Group B 2 Xeroderma Pigmentosum, Complementation Group C 2 Xeroderma Pigmentosum, Complementation Group D 2 Xeroderma[] primary teeth eruption, failure of secondary teeth eruption, corneal dystrophy, aggressive behaviour [ 192 – 194 ].[]

  • Congenital Ichthyosis

    J Glaucoma . 2016 Mar. 25 (3):e280-3. [Medline] . Scheers C, Andre J, Thompson C, Rebuffat E, Harag S, Kolivras A.[] Also called fish skin disease, xeroderma. ichthyotic, adj.[] Oral and dental findings reported in itchthyosis patients included gingivitis, periodontitis, enamel hypoplasia, high caries incidence, delayed primary and secondary eruption[]

  • 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[] (hyperdontia) in the primary and secondary dentition resulting in crowding and malocclusion, retention of deciduous teeth, delayed eruption of secondary dentition and failure[] […] posterior polar, 1 * Cataract, posterior polar, 5 * Cataract, total congenital * Cataract, zonular * Cataract,posterior polar, 3 * Cataract,posterior polar, 4 * Cataract-glaucoma[]

  • X-Linked Mandibulofacial Dysostosis

    Cataracts and glaucoma require attention when present, of course.[] Ectodermal Dysplasia Rapp-Hodgkin Ectodermal Dysplasia Tricho-Dento-Osseous Syndrome Clouston Syndrome Cranioectodermal Dysplasia GAPO Syndrome Pachyonychia Congenita Syndrome Xeroderma[] […] or completefailure of eruption of permanent teethHistology:Unerupted permanent teeth lack secondary cementumTreatment:No treatment; full-mouth extractions with denture construction[]

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

    Glaucoma develops in 50-70% of patients with Lowe syndrome, usually by age 6 years.[] […] syndrome Autosomal dominant intermediate Charcot-Marie-Tooth Genitopatellar syndrome Keratoderma palmoplantar deafness Congenital primary aphakia Russell-Silver syndrome Xeroderma[] : delayed eruption of primary teeth alveolar process hypoplasia multiple non-erupting secondary teeth pseudoanodontia Skeletal Limbs: genu valga Clinical features from OMIM[]

  • Progeroid Facial Appearance with Hand Anomalies

    […] dysplasia/detachment, cataracts, optic atrophy, other ocular abnormalities Oculodentodigital dysplasia (164200) Microcornea, short palpebral fissures, epicanthal folds, glaucoma[] Photosensitivity, especially congenital, e.g. poikiloderma congenitale, xeroderma pigmentosum, Cockayne‘s syndrome. Diseases causing elastolysis, e.g. cutis laxa.[] Dental abnormalities may also be present, such as delayed eruption of the primary (deciduous) and secondary (permanent) teeth; irregularly formed, small, discolored, and/or[]

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