Create issue ticket

135 Possible Causes for Anterior Fontanelle Closure Delayed

  • Mesomelic Dysplasia, Savarirayan Type

    closure of the anterior fontanelle ; Dislocated radial head ; Fibular aplasia ; Global developmental delay ; Hip dislocation ; Mesomelia ; Short stature ; Short tibia ; Talipes[mousephenotype.org] closure of the anterior fontanelle Later than typical closing of soft spot of skull 0001476 Dislocated radial head 0003083 Global developmental delay 0001263 Short tibia[rarediseases.info.nih.gov] FIBULAS AND TRIANGULAR TIBIAS Classification bone, developmental, genetic Phenotypes Abnormality of the foot ; Abnormality of the thorax ; Autosomal dominant inheritance ; Delayed[mousephenotype.org]

  • Nestor-Guillermo Progeria Syndrome

    closure of the anterior fontanelle ; Dental crowding ; Failure to thrive ; Flexion contracture ; Hypertension ; Joint stiffness ; Lipoatrophy ; Malar flattening ; Micrognathia[mousephenotype.org] […] developmental, endocrine, genetic, skin Phenotypes Abnormality of the forearm ; Abnormality of the ribs ; Atherosclerosis ; Autosomal recessive inheritance ; Convex nasal ridge ; Delayed[mousephenotype.org]

  • Kenny-Caffey Syndrome Type 1

    closure of anterior fontanelle, eye abnormalities, and hypoparathyroidism.[ingentaconnect.com] […] the anterior fontanel, eye abnormalities, and transient hypocalcemia.[malacards.org] Alopecia, delayed closure of the anterior fontanel, and apparent thickening of the cortex in long bones may be seen.[disorders.eyes.arizona.edu]

  • Coffin-Lowry Syndrome

    Involvement of the head and neck can present as thickened calvarium, small sinuses paranasales, flat occiput, delayed suture closure with large anterior fontanelle, prominent[accessanesthesiology.mhmedical.com] closure of the anterior fontanelle Later than typical closing of soft spot of skull 0001476 Dental malocclusion Bad bite Malalignment of upper and lower dental arches Misalignment[rarediseases.info.nih.gov] Loose and inelastic skin 0000973 Cutis marmorata 0000965 Decreased body weight Decreased weight Low body weight Low weight Weight less than 3rd percentile [ more ] 0004325 Delayed[rarediseases.info.nih.gov]

  • Canavan Disease

    We report three cases of L-2-hydroxyglutaric acidemia and three cases of Canavan disease. The L-2-hydroxyglutaric acidemia cases are the first biochemically proven Turkish cases. Magnetic resonance imaging findings in the cases and similarities between the two diseases are emphasized. Both diseases are[…][ncbi.nlm.nih.gov]

  • Hypertelorism

    The craniofacial appearance caused by HDAC8 mutations overlaps that of typical CdLS but often displays delayed anterior fontanelle closure, ocular hypertelorism, hooding of[ncbi.nlm.nih.gov]

  • Opitz-Kaveggia Syndrome

    Opitz and Kaveggia [Opitz and Kaveggia (1974); Z Kinderheilkd 117:1-18] reported on a family of five affected males with distinctive facial appearance, mental retardation, macrocephaly, imperforate anus, and hypotonia. Risheg et al. [Risheg et al. (2007); Nature Genetics 39:451-453] identified an identical mutation[…][ncbi.nlm.nih.gov]

  • Dermatosparaxis

    Dermatosparaxis is an autosomal recessive connective tissue disorder in animals that is caused by abnormal processing of type I procollagen and results in skin laxity and fragility. Only three humans with characteristic biochemical and electronmicroscopic findings have been recognized to date. We describe the clinical[…][ncbi.nlm.nih.gov]

  • Cornelia De Lange Syndrome

    The craniofacial appearance caused by HDAC8 mutations overlaps that of typical CdLS but often displays delayed anterior fontanelle closure, ocular hypertelorism, hooding of[ncbi.nlm.nih.gov] Mutations in the HDAC8 gene cause a somewhat different set of features, including delayed closure of the "soft spot" on the head (the anterior fontanelle) in infancy, widely[ghr.nlm.nih.gov]

  • Cutis Laxa, Autosomal Recessive

    anterior fontanelle closure), hypoplastic mandible [Figure 1] , lax skin over abdomen and knees, short phalanges.[ijpd.in] Characteristics of the syndrome include congenital dislocation of the hips, wide patency and delayed closure of the anterior fontanel, and delayed intrauterine growth and[pediatrics.aappublications.org] Other features seen include growth retardation, flat feet, delayed closure of the anterior fontanel, a typical facial appearance with down-slanting palpebral fissures, and[cags.org.ae]

Further symptoms