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112 Possible Causes for Delayed Closure of Fontanelles, Speech Delay

  • Monosomy 1p36 Syndrome

    […] of speech development Delayed language development Delayed speech Delayed speech acquisition Delayed speech development Impaired speech and language development Impaired[] Smith-Magenis Syndrome – deletion of the 17p11.2 regions leads to mental retardation, hypotonia, speech delay and sleeping disorders.[] Characterised by hypotonia, absent or severely delayed speech and autistic behaviour.[]

  • Russell-Silver Syndrome

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

  • Rubinstein-Taybi Syndrome

    […] of speech development Delayed language development Delayed speech Delayed speech acquisition Delayed speech development Impaired speech and language development Impaired[] 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[] Most children with RSTS experience a significant delay in expressive speech.[]

  • Tenorio Syndrome

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

  • Cleidocranial Dysplasia

    Speech and language may also need to be assessed by a speech pathologist. Genetic counseling may be of benefit for patients and their families.[] Abstract Cleidocranial dysplasia (CCD) is a rare genetic disorder of bone, characterised by hypoplastic/aplastic clavicles, delayed closure of fontanelles and sutures of the[] 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[]

  • Primary Hypertrophic Osteoarthropathy

    Delayed suture closure and late motor development and speech/language were observed. Physical examination also identified hyperhidrosis of the hands.[] 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[] Abstract Autosomal recessive primary hypertrophic osteoarthropathy1 (PHOAR1) is characterized by delayed closure of the fontanels, digital clubbing, arthropathy and periostosis[]

  • Saethre-Chotzen Syndrome

    Benji was diagnosed with speech developmental delay when he moved to the third foster family.[] closure of large fontanels, brachycephaly, acrocephaly, brachydactyly, cutaneous syndactyly, broad great toes, and mild shortness of stature.[] If we find developmental delays, we carefully assess your child to recommend treatments and services.[]

  • Microcephalic Osteodysplastic Primordial Dwarfism Types 1 and 3

    […] problems, including difficulty forming clear words (verbal dyspraxia) and delayed speech Though smaller than normal, individuals with this syndrome are generally taller than[] […] bone age, downturned corners of mouth and thin upper lip, hypospadias , high pitched voice, small chin, delayed closure of the fontanel , hypoglycemia , and a bossed forehead[] closure of the fontanel, hypoglycemia, and a broadforehead which may appear to be triangular shaped and largefor their small body size, and some patients have hemi-hyper-trophy[]

  • Kenny-Caffey Syndrome Type 1

    Articulaton defect Mild articulation problem Delayed speech Stertor Mild No No Latest weight 5500 GMS 6400 GMS 7200 GMS Radiological findings Nephrocalcinosis Nephrocalcinosis[] Clinical features include cortical thickening and medullary stenosis of the tubular bones, delayed closure of fontanels, defective dentition, small eyes with hypermetropia[] All of our patients showed the cardinal features described previously Neurological manifestations in the form of microcephaly, developmental delay, mental retardation, and[]

  • Dysostosis

    Their progress should be carefully monitored and educators should be informed of the potential for delayed onset of speech and difficulties with speech development including[] Other symptoms can include: Ability to touch shoulders together in front of body Delayed closure of fontanelles ("soft spots") Loose joints Prominent forehead ( frontal bossing[] All affected family members had normal psychomotor development and normal intelligence with the exception of subject V.4 who had delayed speech acquisition and started to[]

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