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2,016 Possible Causes for Craniosynostosis, Defect in Dentin Maturation, Flattening of the Talar Dome

  • X-Linked Hypophosphatemia

    […] shortening of the talar neck and flattening of the talar dome.[ncbi.nlm.nih.gov] Delayed dentition; dental abscesses; deafness; Chiari malformation; extraskeletal calcification of the tendons, ligaments, and joint capsules; and craniosynostosis are occasionally[emedicine.com] Other features of the disease include dental abscesses, early tooth decay, craniosynostosis and hypertension.[austinpublishinggroup.com]

  • Hypophosphatasia

    TNAP was found to be highly expressed by mature odontoblasts, and Alpl(-/-) molar and incisor roots featured defective dentin mineralization, ranging from a mild delay to[ncbi.nlm.nih.gov] Craniosynostosis is accompanied by putatively functional consequences.[ncbi.nlm.nih.gov] Patients with HPP have defective bone mineralization as well as craniosynostosis that can be seen in the infantile and childhood forms of this disease.[ncbi.nlm.nih.gov]

    Missing: Flattening of the Talar Dome
  • X-Linked Mandibulofacial Dysostosis

    .• Defect in the maturation of enamel • Mottled brown crystals • Chipping from dentin with an explorer• Normal shape • Very uncommon anterior open bite• Mottled appearance[slideshare.net] Apert syndrome 101200 AD craniosynostosis, brachysphenocephalic acrocephaly, flat facies, high narrow palate Pfeiffer syndrome 101600 AD mild craniosynostosis, flat facies[widesmiles2.org] […] in bone, dentin, ligaments, skin and sclera caused by defective collagen synthesis and maturation Osteogenesis Imperfecta: Mild cases/ congenital form In mildest cases, individuals[quizlet.com]

    Missing: Flattening of the Talar Dome
  • Crouzon Syndrome

    Craniosynostosis can happen before the baby is born or during the first few months of life.[sickkids.ca] Craniosynostosis: genes and mechanisms.[ncbi.nlm.nih.gov] (FGFR 2) gene, and characterized by craniosynostosis, shallow orbits, ocular proptosis, midface hypoplasia and a curved, beak‑like nose.[ncbi.nlm.nih.gov]

    Missing: Defect in Dentin Maturation Flattening of the Talar Dome
  • Brachycephaly

    For this same photo without the arrows, click here For more information, click on the link if you see this icon Pediatric craniosynostosis. eMedicine.[learningradiology.com] This is known as craniosynostosis.[nhs.uk] A boy with brachycephaly without craniosynostosis, raised intracranial pressure, deafness, cataracts, and global developmental delay is described.[ncbi.nlm.nih.gov]

    Missing: Defect in Dentin Maturation Flattening of the Talar Dome
  • Mucopolysaccharidosis

    We present the first reported case associating MPS-I (Hurler-Scheie subtype) with craniosynostosis. A 2.5-year-old girl presented initially with macrocrania.[ncbi.nlm.nih.gov] […] syndrome with variable manifestations exhibiting mainly microcephaly, characteristic facies, mental retardation, short stature, acral skeletal anomalies with occasional craniosynostosis[icd9data.com]

    Missing: Defect in Dentin Maturation Flattening of the Talar Dome
  • Mandibulofacial Dysostosis

    In conclusion, in children with syndromic or complex craniosynostosis, diagnosing OSA using home cardiorespiratory monitoring is feasible.[doi.org] Apert syndrome (Medical Encyclopedia) Cleidocranial dysostosis (Medical Encyclopedia) Craniosynostosis (Medical Encyclopedia) Craniosynostosis repair (Medical Encyclopedia[icdlist.com] Congenital craniofacial differences are conditions affecting the head and face that present at or shortly after birth such as craniosynostosis, cleft lip and palate, hemifacial[eng.ichacha.net]

    Missing: Defect in Dentin Maturation Flattening of the Talar Dome
  • Saethre-Chotzen Syndrome

    Furthermore, craniosynostosis was not present at birth or at the age of 4 months.[ncbi.nlm.nih.gov] Craniosynostosis can happen before the baby is born or during the first few months of life.[sickkids.ca] Abstract Craniosynostosis or premature closure of the cranial sutures is a common abnormality occurring in about 1 in 2500 children.[ncbi.nlm.nih.gov]

    Missing: Defect in Dentin Maturation Flattening of the Talar Dome
  • Acrocephalopolysyndactyly

    […] sagittal craniosynostosis lambdoid sutures craniosynostosis pilonidal dimple absent coccyx spina bifida occulta scoliosis coxa v alga decreased hip-joint mobility flared[humpath.com] * Англо-русский медицинский словарь См. также в других словарях: acrocephalopolysyndactyly — A group of congenital syndromes characterized by abnormal skull shape due to craniosynostosis[translate.academic.ru] […] acrocephalopolysyndactyly (s) ( noun ), acrocephalopolysyndactylies (pl) Any of four heritable malformation syndromes recognizable at birth and characterized by premature craniosynostosis[wordinfo.info]

    Missing: Defect in Dentin Maturation Flattening of the Talar Dome
  • Pallister-Hall Syndrome

    Craniosynostosis was noted in several of the earliest GCPS case reports, but we have observed this in very few patients.[ojrd.biomedcentral.com] Other, less common anomalies in GCPS include craniosynostosis, mental retardation, agenesis of the corpus callosum, and umbilical and diaphragmatic hernias.[ojrd.biomedcentral.com] Keywords Craniosynostosis Polydactyly Denature High Performance Liquid Chromatography Nevoid Basal Cell Carcinoma Syndrome Gorlin Syndrome Disease name, synonyms, and included[ojrd.biomedcentral.com]

    Missing: Defect in Dentin Maturation Flattening of the Talar Dome

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