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22 Possible Causes for Delayed Eruption of Primary and Secondary Teeth, Dysmorphic Face, Skeletal Dysplasia

  • Cleidocranial Dysplasia

    Cleidocranial dysostosis (CCD) is a rare skeletal dysplasia with predominantly membranous bone involvement. It carries an autosomal dominant inheritance 4.[web.archive.org] […] shedding of primary teeth and also eruption of secondary teeth.[ncbi.nlm.nih.gov] The patient's family history showed his father and eldest daughter with similar dysmorphic faces, skeletal disorders and proximal upper extremity weakness.[ncbi.nlm.nih.gov]

  • SHORT Syndrome

    Children with a skeletal dysplasia, or chondrodystrophy, are short and have abnormal body proportions; intelligence is normal.[hgfound.org] 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] We report the two-year-four-month old female with SHORT syndrome who present growth retardation and dysmorphic features (triangular-shaped face, prominent forehead, ocular[ncbi.nlm.nih.gov]

  • Familial Short Stature

    Thanatophoric dysplasia It is the most common lethal skeletal dysplasia in the neo‐natal period.[intechopen.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] Dysmorphic features: Trisomy 21: hypotonia, upward slanting of palpebral fissures, round face, micrognathia, single palmar crease, brachycephaly Turner syndrome: webbed neck[online.epocrates.com]

  • Oculodentodigital Dysplasia

    dysplasia, enamel dysplasia, and hypotrichosis.[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] We report a case of a 6-year-old male who presented with dysmorphic facial features (short palpebral fissure, thin nose with hypoplastic alae nasi, and flat face), bilateral[ncbi.nlm.nih.gov]

  • Crane-Heise Syndrome

    The combination of skeletal dysplasia, seizure disorder and Crane-Heise Syndrome require Faith to wear a soft-shelled helmet because she does not have a cranial cap.[youcaring.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] Mental Retardation, Microcephaly, Epilepsy, and Coarse Face Mental Retardation, Microcephaly, Growth Retardation, Joint Contractures, and Facial Dysmorphism Mental Retardation[rgd.mcw.edu]

  • X-Linked Mandibulofacial Dysostosis

    The skeletal dysplasias The skeletal dysplasias are disorders associated with a generalized abnormality in the skeleton.[nature.com] […] or completefailure of eruption of permanent teethHistology:Unerupted permanent teeth lack secondary cementumTreatment:No treatment; full-mouth extractions with denture construction[slideshare.net] Fumarase deficiency Galloway-Mowat syndrome Genitopatellar syndrome Glass syndrome Goldberg-Shprintzen megacolon syndrome GRACILE syndrome Greenberg skeletal dysplasia Greig[qlinics.com]

  • Apert Syndrome

    The role of the human fibroblast growth factor receptor (FGFR) gene family in current prenatal diagnosis and management of craniosynostosis syndromes and skeletal dysplasias[ncbi.nlm.nih.gov] The delayed eruption may be secondary to the crowding, stacking, and displacement of the teeth within the alveolus, which is often wide to accommodate the tooth buds in two[head-face-med.biomedcentral.com] dysplasias.[ncbi.nlm.nih.gov]

  • Micrognathism

    Yunis Varón syndrome is a rare skeletal dysplasia. It is thought to be autosomal recessive.[radiopaedia.org] (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] face is mandatory, associated to another major criteria or two minor criteria.[ncbi.nlm.nih.gov]

  • Gingival Fibromatosis-Progressive Deafness Syndrome

    22q11.2 deletion syndrome Thanatophoric dysplasia type 2 Familial partial lipodystrophy Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia[checkrare.com] primary teeth eruption, failure of secondary teeth eruption, corneal dystrophy, aggressive behaviour [ 192 – 194 ].[ojrd.biomedcentral.com] Cataracts, Hearing Loss, and Neurodegeneration 1 Congenital Central Hypoventilation syndrome 11 Congenital Contractural Arachnodactyly 6 Congenital Contractures of the Limbs and Face[preventiongenetics.com]

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

    Chondroectodermal dysplasia. J Bone Joint Surg 44-B: 626, 1962. Kaitila, I.I., Leisti, J.T., Rimoin, D.L. Mesomelic skeletal dysplasias.[gait.aidi.udel.edu] : delayed eruption of primary teeth alveolar process hypoplasia multiple non-erupting secondary teeth pseudoanodontia Skeletal Limbs: genu valga Clinical features from OMIM[malacards.org] (including round face, frontal bossing, antimongoloid slant of the eyes, epicanthal folds, large low set ears, broad nasal base, anteverted nostrils, and long upper lip).[ncbi.nlm.nih.gov]

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