Create issue ticket

412 Possible Causes for Delayed Closure of Fontanelles, Mild Maxillary Prognathism

  • Saethre-Chotzen Syndrome

    closure of large fontanels, brachycephaly, acrocephaly, brachydactyly, cutaneous syndactyly, broad great toes, and mild shortness of stature.[ncbi.nlm.nih.gov] The leptoprosopic flat face with mild maxillary hypoplasia and relative mandibular prognathism was exemplified by a prominent chin [ Figure 2 ].[ncbi.nlm.nih.gov] Note maxillary hypoplasia, ocular proptosis with mild relative prognathism. (From Renier et al. 2000) syndrome is genetically heterogeneous.[rrnursingschool.biz]

  • Cleidocranial Dysplasia

    Cleidocranial dysplasia (CCD) is a rare genetic disorder of bone, characterised by hypoplastic/aplastic clavicles, delayed closure of fontanelles and sutures of the cranium[ncbi.nlm.nih.gov] We studied a Chinese family that included three affected individuals with CCD phenotypes; the clinical features of patients with CCD include delayed closure of fontanelles[ncbi.nlm.nih.gov] CCD is an autosomal skeletal disorder characterized by several features such as delayed closure of fontanels, dental abnormalities and hypoplastic clavicles.[ncbi.nlm.nih.gov]

    Missing: Mild Maxillary Prognathism
  • Kenny-Caffey Syndrome Type 1

    Clinical features include cortical thickening and medullary stenosis of the tubular bones, delayed closure of fontanels, defective dentition, small eyes with hypermetropia[uniprot.org] OMIM : 57 Kenny-Caffey syndrome is characterized by severe proportionate short stature, cortical thickening and medullary stenosis of the tubular bones, delayed closure of[malacards.org] […] the anterior fontanel, eye abnormalities, and transient hypocalcemia.[malacards.org]

    Missing: Mild Maxillary Prognathism
  • Micrognathism

    Symptoms INHERITANCE: Autosomal recessive GROWTH: [Height]; Short stature HEAD AND NECK: [Head]; Large anterior fontanel; Delayed closure anterior fontanel; [Face]; Micrognathia[findzebra.com] […] of the teeth -Mild prognathism www.indiandentalacademy.com 19.  Hypoparathyroidism - retarded eruption -early exfoliation -enamel defects  Hyperparathyroidism - demineralization[slideshare.net] Symptoms INHERITANCE: X-linked dominant GROWTH: [Height]; Short to normal stature; [Other]; Failure to thrive HEAD AND NECK: [Head]; Delayed closure of fontanel; [Face]; Small[findzebra.com]

  • Autosomal Recessive Pachydermoperiostosis 

    Currarino's disease is an extremely rare variant of primary hypertrophic osteoarthropathy in which there is delayed closure of the fontanelles and an absence of skin involvement[ncbi.nlm.nih.gov] Autosomal recessive primary hypertrophic osteoarthropathy1 (PHOAR1) is characterized by delayed closure of the fontanels, digital clubbing, arthropathy and periostosis.[ncbi.nlm.nih.gov] We have now encountered three siblings, two of whom had digital clubbing, patent arterial ducts and delayed closure of the cranial fontanels.[ncbi.nlm.nih.gov]

    Missing: Mild Maxillary Prognathism
  • Cranio-Osteo-Arthropathy

    closure of the cranial sutures and fontanels, resulting in wide fontanels, and an increased number of wormian bones.[orpha.net] They typically present earlier in childhood and have delayed neurocranial ossification, with delayed closure of the fontanelles, and may also have congenital heart disease[dvkeywords.blogspot.com] closure of the fontanels, periostosis, and variable patent ductus arteriosus.[genecards.org]

    Missing: Mild Maxillary Prognathism
  • Vitamin D Deficiency

    […] dentition, delayed anterior fontanelle closure Investigations Infants Infants: Exclusively breastfed infants with at least one other risk factor without symptoms/signs -[rch.org.au] […] tooth eruption (no incisors by aged 10 months, no molars by age 18 months) - Craniotabes (softening of skull bones) - Delayed closure of anterior fontanelle - Frontal bossing[starship.org.nz] In older infants with rickets, sitting and crawling are delayed, as is fontanelle closure; there is bossing of the skull and costochondral thickening.[merckmanuals.com]

    Missing: Mild Maxillary Prognathism
  • Pyknodysostosis

    closure of the fontanelles, and hypoplasia of the terminal phalanges.[medical-dictionary.thefreedictionary.com] Pyknodysostosis Description, Causes and Risk Factors: A condition characterized by short stature, delayed closure of the fontanels, and hypoplasia of the terminal phalanges[medigoo.com] closure of the fontanelles, and hypoplasia of the terminal phalanges; autosomal recessive inheritance.[medical-dictionary.thefreedictionary.com]

    Missing: Mild Maxillary Prognathism
  • Familial Scaphocephaly Syndrome

    Unusual raised ridges on the skull Premature closure of sutures; Synostosis; Plagiocephaly; Scaphocephaly; Fontanelle - craniosynostosis; Soft spot - craniosynostosis Centers[medlineplus.gov] Note maxillary hypoplasia, ocular proptosis with mild relative prognathism. (From Renier et al. 2000) syndrome is genetically heterogeneous.[rrnursingschool.biz] Complications may include: Increased intracranial pressure Seizures Developmental delay Call your child's provider if your child has: Unusual head shape Problems with growth[medlineplus.gov]

  • Baller-Gerold Syndrome

    Characterization of a new syndrome that associates craniosynostosis, delayed fontanel closure, parietal foramina, imperforate anus, and skin eruption: CDAGS.[ncbi.nlm.nih.gov] Note maxillary hypoplasia, ocular proptosis with mild relative prognathism. (From Renier et al. 2000) syndrome is genetically heterogeneous.[rrnursingschool.biz]

Further symptoms

Similar symptoms