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18 Possible Causes for Delayed Eruption of Primary and Secondary Teeth, Hyperpigmentation

  • Bloch Sulzberger Syndrome

    It is characterized by swirled patterns of hyperpigmentation.[] 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[] The blisters heal gradually, but leave behind areas of hyperpigmentation over the skin.[]

  • Carney Complex

    We report an illustrated case of a 61-year-old woman with multiple atrial myxomas and cutaneous hyperpigmentation as part of the Carney complex.[] This syndrome includes dental defects, such as persistent primary teeth, delayed eruption of secondary teeth, oligodontia, elongated roots with open apices and enamel hypoplasia[] Carney complex and its subsets LAMB syndrome and NAME syndrome are autosomal dominant conditions comprising myxomas of the heart and skin, hyperpigmentation of the skin (lentiginosis[]

  • Cleidocranial Dysplasia

    Progressively stiff joints Acroosteodysplasia of fingers & toes w/delayed ossification of carpal bones Micrognathia Early tooth loss Atrophic skin w/ subcutaneous fat Acroosteolysis Hyperpigmentation[] […] shedding of primary teeth and also eruption of secondary teeth.[] […] joints Acroosteodysplasia of fingers & toes w/delayed ossification of carpal bones Micrognathia Early tooth loss Atrophic skin w/decreased subcutaneous fat Acroosteolysis Hyperpigmentation[]

  • Gingival Fibromatosis-Progressive Deafness Syndrome

    Multiple impacted teeth Plantar hyperkeratosis Hepatoblastoma Adrenocortical adenoma Medulloblastoma Brain neoplasm Hamartomatous polyposis Melanoma Fibroma Precocious puberty Hyperpigmentation[] primary teeth eruption, failure of secondary teeth eruption, corneal dystrophy, aggressive behaviour [ 192 – 194 ].[] […] hemoglobinopathy Genetic hemophagocytic lymphohistiocytosis Genetic hyperaldosteronism Genetic hyperferritinemia without iron overload Genetic hyperparathyroidism Genetic hyperpigmentation[]

  • Progeria

    […] clinical features were observed, including presenile manifestations such as bird-like facial appearance, generalized lipodystrophy involving the extremities and mottled hyperpigmentation[] Dental abnormalities may also be present, such as delayed eruption of the primary (deciduous) and secondary (permanent) teeth; irregularly formed, small, discolored, and/or[] […] stature, alopecia, craniofacial disproportion, micrognathia, hypoplastic mandible, beak-like nose, decreased subcutaneous fat, atrophic skin, sclerodermoid lesion, mottling hyperpigmentation[]

  • Familial Congenital Nasolacrimal Duct Obstruction

    […] area 374.50 Degenerative disorder of eyelid, unspecified 374.51 Xanthelasma Xanthoma (planum) (tuberosum) of eyelid Code first underlying condition (272.0-272.9) 374.52 Hyperpigmentation[] 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[] Diffuse Idiopathic Skeletal Hyperostosis, Sternocostoclavicular Hyperoxaluria Hyperoxaluria, Primary Hyperoxia Hyperparathyroidism Hyperparathyroidism, Secondary Hyperphagia Hyperpigmentation[]

  • Oculodentodigital Dysplasia

    Syndrome Hutterite Cerebroosteonephrodysplasia Syndrome hydrolethalus syndrome hypereosinophilic syndrome Hyperimmunoglobulin G1(A1) Syndrome hyperinsulinism Hyperkeratosis-Hyperpigmentation[] Dental conditions frequently seen with this condition include: delayed eruption of primary or secondary (permanent) teeth, crowded/misaligned teeth, and increased incidence[]

  • Ichthyosis

    It is characterized in affected females by cicatricial scarring, alopecia, patchy or diffuse ichthyosis that may resolve into atrophoderma and hyperpigmentation, punctuate[] Oral and dental findings reported in itchthyosis patients included gingivitis, periodontitis, enamel hypoplasia, high caries incidence, delayed primary and secondary eruption[] , bruxism, bifid teeth, the irregular morphology of teeth, fish mouth appearance, mouth breathing, xerostomia, and hyperkeratotic plaques on the tongue. [2], [12], [15], [[]

  • Gingival Fibromatosis-Hypertrichosis Syndrome

    This study describes a patient with ZLS with novel findings, including colpocephaly, hemivertebra, polydactyly, hyperpigmentation, and hemihyperplasia.[] primary teeth eruption, failure of secondary teeth eruption, corneal dystrophy, aggressive behaviour [ 192 – 194 ].[] Publication Analysis Top Keywords zimmermann-laband syndrome 8 colpocephaly hemivertebra 4 hemivertebra polydactyly 4 polydactyly hyperpigmentation 4 References (Supplied[]

  • Crane-Heise Syndrome

    Syndrome Huntington's Disease-Like Syndrome Hutterite Cerebroosteonephrodysplasia Syndrome hypereosinophilic syndrome Hyperimmunoglobulin G1(A1) Syndrome Hyperkeratosis-Hyperpigmentation[] (hyperdontia) in the primary and secondary dentition resulting in crowding and malocclusion, retention of deciduous teeth, delayed eruption of secondary dentition and failure[] […] syndrome deficiency XLAG Cleft lip and/or palate with mucous Glutamate-cysteine ligase Mental retardation hypotonia skin Pyruvate dehydrogenase cysts of lower lip deficiency hyperpigmentation[]

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