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24 Possible Causes for Delayed Eruption of Primary and Secondary Teeth, Turner Syndrome

  • Familial Short Stature

    Ellison JW et al. (1997) PHOG, a candidate gene for involvement in the short stature of Turner syndrome. [ ] 14.[moldiag.com] The eruption of primary and secondary teeth may be delayed for up to 1.3 years in children with growth hormone deficiency, 16 up to 1.5 years in children with constitutional[aafp.org] Syndrome 2281 Genetics and Growth Response to Growth Hormone Treatment in Comparison with Turner Syndrome 2299 138 Zinc Transporter Mutations and Human Growth 2319 139 Growth[books.google.com]

  • SHOX-Related Short Stature

    Turner syndrome—2008. Horm Res, 71 (2009), pp. 52-56 [2] M.L. Davenport. Approach to the patient with Turner syndrome.[elsevier.es] 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[patient.info] Not all girls with Turner syndrome need treatment with somatropin. Turner syndrome occurs in between 1 in 1500 and 1 in 2500 live female births.[nice.org.uk]

  • Micrognathism

    Conclusion: The results of this study suggest that karyotype variations might affect phenotype of Turner syndrome.[ijms.sums.ac.ir] (hyperdontia) in the primary and secondary dentition resulting in crowding and malocclusion, retention of deciduous teeth, delayed eruption of secondary dentition and failure[findzebra.com] syndrome type 1 Trichorhinophalangeal syndrome type 3 Turner's syndrome Van Bogaert-Hozay syndrome Wagner vitreoretinal degeneration syndrome Weissenbacher-Zweymuller syndrome[wikidoc.org]

  • SHORT Syndrome

    Girls with Turner syndrome may have difficulty settling in class.[nhs.uk] 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[patient.info] The intelligence of those with Turner syndrome is usually within the normal range.[medicinenet.com]

  • Brachydactyly Type E

    Turner syndrome, Albright hereditary osteodystrophy, hypertension with brachydactyly, chromosome 2q37 microdeletion and PTHLH mutations were excluded following clinical, biochemical[ncbi.nlm.nih.gov] In a subgroup of BDE with mutations in PTHLH , abnormalities of dentition may occur, including oligodontia and delayed eruption of the primary and secondary teeth.[link.springer.com] Abnormally short digits involving the metacarpals, classified as brachydactyly type E, can be isolated or occur as part of a syndrome.[ncbi.nlm.nih.gov]

  • Familial Congenital Nasolacrimal Duct Obstruction

    […] and Turner’s syndrome.[calvarypediatrics.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] […] may be associated with trisomy 13, Turner syndrome, Cornelia de Lange syndrome, Noonan syndrome and Baraitser-Winter syndrome, among others. 4,5 Autosomal-dominant blepharophimosis-ptosis-epicanthus[reviewofophthalmology.com]

  • Gingival Fibromatosis-Progressive Deafness Syndrome

    , Craniofaciocutaneous syndrome, LEOPARD syndrome, Neurofibromatosis type 1, SPRED1 spectrum Chromosomal abnormalities including X-/XY mosaicism, Turner syndrome Fetal hydantoin[centogene.com] primary teeth eruption, failure of secondary teeth eruption, corneal dystrophy, aggressive behaviour [ 192 – 194 ].[ojrd.biomedcentral.com] […] carboxylase 1 deficiency Wilson-Turner syndrome Cleft palate, midfacial hypoplasia, triangular facies, and sensorineural hearing loss Becker muscular dystrophy Spinocerebellar[checkrare.com]

  • X-Linked Mandibulofacial Dysostosis

    Morbus Down Morfan (Mental Retardation-Pre- And Postnatal Overgrowth-Remarkable Face-Acanthosis Nigricans) Syndrome Morgagni-Turner Syndrome Morgagni-Turner-Albright Syndrome[neo-genetics.com] […] or completefailure of eruption of permanent teethHistology:Unerupted permanent teeth lack secondary cementumTreatment:No treatment; full-mouth extractions with denture construction[slideshare.net] Originally thought to be a variant of Turner Syndrome- used to be referred to as “male version of Turner Syndrome” Autosomal Dominant PTPN11 gene (12q24) Clinical Findings[slideplayer.com]

  • Coffin-Lowry Syndrome

    Patients with Down’s syndrome may have subglottic stenosis, macroglossia, and atlanto-axial instability. Patients with Turner’s syndrome may have micrognathia (2) .[journals.lww.com] Dental anomalies are common and include small teeth, malpositioning, open bite, hypodontia of secondary teeth, advanced or delayed eruption of primary teeth, and premature[ncbi.nlm.nih.gov] syndrome 759.89 Rubinstein-Taybi's syndrome (brachydactylia, short stature and intellectual disabilities) 759.89 Rud's syndrome (mental deficiency, epilepsy, and infantilism[icd9data.com]

  • Carney Complex

    Turner’s Syndrome This Topic on the Message Boards . V Von Hippel-Lindau disease This Topic on the Message Boards .[cushieblog.com] This syndrome includes dental defects, such as persistent primary teeth, delayed eruption of secondary teeth, oligodontia, elongated roots with open apices and enamel hypoplasia[nature.com] Turner , Multiple lentigines associated with cutaneous myxomas, Journal of the American Academy of Dermatology , 2001 , 44 , 2, 282 CrossRef 20 A. Gentil Baldrich , T.[onlinelibrary.wiley.com]

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