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195 Possible Causes for Anterior Fontanelle Open in Adults, Delayed Closure of Fontanelles

  • 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]

  • 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]

  • Primary Hypertrophic Osteoarthropathy

    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: Anterior Fontanelle Open in Adults
  • Russell-Silver Syndrome

    […] of the anterior fontanel (soft spot) · frequent ear infections or chronic fluid in ears · congenital absence of the second premolars · delay of gross and fine motor development[coltongeorge.com] […] resulting in vomiting or frequent spitting up c) slow movement of the small intestine &/or large intestine (constipation) · blue sclera (bluish tinge in white of eye) · late closure[coltongeorge.com]

    Missing: Anterior Fontanelle Open in Adults
  • Saethre-Chotzen Syndrome

    closure of large fontanels, brachycephaly, acrocephaly, brachydactyly, cutaneous syndactyly, broad great toes, and mild shortness of stature.[ncbi.nlm.nih.gov] Abstract A family is described in which 15 persons in five generations are affected with a complex of skeletal malformations which variably includes peculiar asymmetric facies, delayed[ncbi.nlm.nih.gov]

    Missing: Anterior Fontanelle Open in Adults
  • Lenz-Majewski Syndrome

    Characterized by multiple congenital anomalies (delayed closure of fontanel, proximal symphalangism, prominent scalp cutaneous veins), mental retardation, and progressive[accessanesthesiology.mhmedical.com] Spanish displasia de Lenz - Majewski English Delayed closure of fontanel, proximal symphalangism, prominent cutaneous veins,mental retardation, and progressive skeletal sclerosis[mymemory.translated.net] Delayed closure of fontanelle, proximal symphalangism, short digits, partial syndactyly, prominent cutaneous veins, loose and wrinkled atrophic skin of hands, skin hypoplasia[accessanesthesiology.mhmedical.com]

    Missing: Anterior Fontanelle Open in Adults
  • Monosomy 1p36 Syndrome

    closure of the anterior fontanelle Later than typical closing of soft spot of skull 0001476 Delayed CNS myelination 0002188 Delayed skeletal maturation Delayed bone maturation[rarediseases.info.nih.gov] […] opening between the eyelids 0000581 Cleft upper lip Harelip 0000204 Congenital hypothyroidism Underactive thyroid gland from birth 0000851 Cranial nerve VI palsy 0006897 Delayed[rarediseases.info.nih.gov]

    Missing: Anterior Fontanelle Open in Adults
  • Autosomal-Recessive Robinow Syndrome

    Am J Med Genet A. 2015 Dec;167A(12):3054-61. doi: 10.1002/ajmg.a.37287. Epub 2015 Aug 18. Aglan M 1, 2 , Amr K 2, 3 , Ismail S 1, 2 , Ashour A 1, 2 , Otaify GA 1, 2 , Mehrez MA 2, 4 , Aboul-Ezz EH 2, 5 , El-Ruby M 1, 2 , Mazen I 1, 2 , Abdel-Hamid MS 2, 3 , Temtamy SA 1, 2 . Author information 1 Department of Clinical Genetics,[…][ncbi.nlm.nih.gov]

    Missing: Anterior Fontanelle Open in Adults
  • Rubinstein-Taybi Syndrome

    Health Soc Work. 2017 Feb 1;42(1):e32-e43. doi: 10.1093/hsw/hlw062. Author information 1 School of Social Work, Robert Stempel College of Public Health and Social Work, Florida International University, 11200 SW 8th Street, Miami, FL, USA. 2 Department of Social and Behavioral Sciences, Harvard T. H. Chan School of Public[…][ncbi.nlm.nih.gov]

    Missing: Anterior Fontanelle Open in Adults
  • 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: Anterior Fontanelle Open in Adults

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