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222 Possible Causes for Delayed Closure of Fontanelles, Speech Delay

  • Osteopathia Striata

    speech and language development Deficiency of speech development Delayed language development Delayed speech Delayed speech acquisition Delayed speech development Impaired[rarediseases.info.nih.gov] closure of the anterior fontanelle ... ...[familydiagnosis.com] closure of anterior fontanelle, large fontanelle, frontal bossing, widened sutures, bitemporal narrowing, micrognathia, hydrocephalus, headaches, speech delay (10%), transitional[iofbonehealth.org]

  • Incontinentia Pigmenti Achromians

    Other significant neurologic complications included hypotonia, macrocephaly, microcephaly, speech delay, autistic behaviors, and expressive language disabilities.[file.scirp.org] Nephew and maternal grandmother Epileptic seizures, retardation, macrocephaly, delayed closure anterior fontanelle, leg length discrepancy, scoliosis and iridial heterochromia[jmedicalcasereports.biomedcentral.com]

  • Trisomy 20

    They may have speech delay, such as saying words later than their peers. People with trisomy 20p usually have mild to moderate intellectual disability.[thinkgenetic.com] Clinical examination of the baby showed only minor phenotypic signs (bilateral epicanthal folds, delayed closure of fontanel with no other gross anomalies), but demonstrated[ncbi.nlm.nih.gov] Speech was particularly delayed and there were difficulties with articulation; his first words appearing at 2½ years with slow progression.[jmg.bmj.com]

  • Tenorio Syndrome

    Involvement of central nervous system presents with variable degrees of intellectual disability, motor delay and speech delay.[orpha.net] Dentition is delayed. Recurrent stomatitis and gastroesophageal reflux have been noted. Closure of the fontanels is delayed.[disorders.eyes.arizona.edu] […] cranial suture closure Mandibular prognathia Wide nose Anteverted nares Telecanthus Thick eyebrow Anxiety Delayed speech and language development Osteopenia Hypertrichosis[familydiagnosis.com]

  • Monosomy 1p36 Syndrome

    […] of speech development Delayed language development Delayed speech Delayed speech acquisition Delayed speech development Impaired speech and language development Impaired[rarediseases.info.nih.gov] His psychomotor development was severely delayed since birth. He was unable to hold his head or sit by his first birthday, and he had no speech throughout his life.[enlivenarchive.org] Smith-Magenis Syndrome – deletion of the 17p11.2 regions leads to mental retardation, hypotonia, speech delay and sleeping disorders.[cureangelman.org]

  • Rubinstein-Taybi Syndrome

    […] of speech development Delayed language development Delayed speech Delayed speech acquisition Delayed speech development Impaired speech and language development Impaired[rarediseases.info.nih.gov] After two years we suspected some speech delay, but it wasn't until she was three that a geneticist confirmed the unvoiced opinion of our paediatrician that she had Rubinstein-Taybi[rarediseaseday.org] Most children with RSTS experience a significant delay in expressive speech.[rarediseases.org]

  • Craniosynostosis

    delay/disorder, articulation or speech sound production delays/disorders, and whether speech therapy was recommended.[ncbi.nlm.nih.gov] Craniosynostosis and clavicular hypoplasia, delayed closure of the fontanelle, cranial defects, anal and genitourinary abnormalities, and skin (CDAGS), is an infrequent autosomal[ncbi.nlm.nih.gov] Help with feeding, swallowing or speech. Uncover any other developmental delays.[gillettechildrens.org]

  • Russell-Silver Syndrome

    Specific issues include growth failure, severe feeding difficulties, gastrointestinal problems, hypoglycaemia, body asymmetry, scoliosis, motor and speech delay and psychosocial[ncbi.nlm.nih.gov] […] 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] Performance : muscular hypotonia and hypotrophy, rare motor/neuropsychological delay, feeding difficulties, speech delay.[atlasgeneticsoncology.org]

  • Apert Syndrome

    Children with Apert Syndrome often have delayed speech and language development, as well as learning disabilities. They also generally have vision and hearing problems.[mun-h-center.se] Craniosynostosis can lead to acrobrachycephaly or turribrachycephaly with delayed closure of fontanels and a possible impact on brain growth and neurological development.[orpha.net] Many children with Apert syndrome have variable degrees of mental, speech or developmental delays. How is Apert syndrome diagnosed?[childrenscolorado.org]

  • Humero-Ulnar Synostosis

    In particular, speech delay was the dominant developmental problem in childhood. She was unable to speak until 4 years of age.[questia.com] It is characterized by developmental abnormalities in the bones and teeth, including the complete or partial absence of the clavicles, delayed closure of the fontanels, protruding[icd10data.com] We present a case with bilateral congenital radio-ulnar synostosis, speech delay, dimple on shoulders, café au lait spot and characteristic facial appearance.[questia.com]

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