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10 Possible Causes for Cognitive Developmental Delay, Mild Maxillary Prognathism

  • Chromosome 22q13.3 Deletion Syndrome
  • Isolated Trigonocephaly

    If left untreated, this can cause increased pressure within the skull (intracranial pressure) and can potentially result in cognitive impairment or developmental delays.[rarediseases.org] Note maxillary hypoplasia, ocular proptosis with mild relative prognathism. (From Renier et al. 2000) syndrome is genetically heterogeneous.[rrnursingschool.biz] The child is now almost five years old with some improvement in his global developmental delay (Figure 2d).[alliedacademies.org]

  • Peters Anomaly

    Developmental delay is observed in 78%-83% of children.[ncbi.nlm.nih.gov] They include mild dysmorphism (hypertelorism, broad flat nose, maxillary hypoplasia, and mild prognathism), dental anomalies (microdontia, hypodontia, anodontia, oligodontia[glaucomatoday.com] Intellectual disability typically ranges from mild to severe, although adults with normal cognitive functioning have been reported.[ncbi.nlm.nih.gov]

  • Craniosynostosis Type 3

    Improperly managed, craniosynostosis can lead to lifelong developmental delays, cognitive impairment and psychosocial difficulties.[sciencebasedmedicine.org] Note maxillary hypoplasia, ocular proptosis with mild relative prognathism. (From Renier et al. 2000) syndrome is genetically heterogeneous.[rrnursingschool.biz]

  • Micrognathism

    Features Skin/Hair Features Other Features PTPN11 Pulmonary valve stenosis Overrepresentation of short stature Little or no cognitive delays ----- ----- PTPN11 Underrepresentation[ncbi.nlm.nih.gov] […] of the teeth -Mild prognathism www.indiandentalacademy.com 19.  Hypoparathyroidism - retarded eruption -early exfoliation -enamel defects  Hyperparathyroidism - demineralization[slideshare.net] […] al, 2011) ( Chart 1 ). 7, 8 Chart 1 Most frequently used medications and potential interactions with systemic antifungals * Gene Cardiovascular Features Growth Features Developmental[ncbi.nlm.nih.gov]

  • Familial Scaphocephaly Syndrome

    If left untreated or ineffectively treated, OSA will result in disabilities that include failure to thrive, recurrent upper respiratory infection, cognitive dysfunction, developmental[pocketdentistry.com] Note maxillary hypoplasia, ocular proptosis with mild relative prognathism. (From Renier et al. 2000) syndrome is genetically heterogeneous.[rrnursingschool.biz] delay, cor pulmonale, and sudden death. 173 Midface hypoplasia in the setting of a craniosynostosis syndrome is often a primary cause of OSA.[pocketdentistry.com]

  • Saethre-Chotzen Syndrome

    But some have learning problems or developmental delays. We will follow your child’s cognitive development closely.[seattlechildrens.org] The leptoprosopic flat face with mild maxillary hypoplasia and relative mandibular prognathism was exemplified by a prominent chin [ Figure 2 ].[ncbi.nlm.nih.gov] Whereas mild-to-moderate developmental delay and intellectual disability have been reported in some individuals with SCS, normal cognitive development is more common.[ncbi.nlm.nih.gov]

  • Robinow-Sorauf Syndrome

    But some have learning problems or developmental delays. We will follow your child’s cognitive development closely.[seattlechildrens.org] The leptoprosopic flat face with mild maxillary hypoplasia and relative mandibular prognathism was exemplified by a prominent chin [Figure 2] .[ijdentistry.com] maxillary hypoplasia and relativemandibular prognathism exemplified by a prominent.Wide root of the nose, thick eyebrows, prominenteyelashes, mild convergent strabismus and[docslide.com.br]

  • Eyebrow Duplication - Syndactyly Syndrome

    FUNCTION, general abnormalities Mental retardation/developmental delay VOICE Voice, general abnormalities Speech delay See also [ edit ] Chromosome 8 (human) References [[en.wikipedia.org] The leptoprosopic flat face with mild maxillary hypoplasia and relative mandibular prognathism was exemplified by a prominent chin [Figure 2].[ijdentistry.com] The feeding difficulties, developmental and cognitive delay, mottled skin, drug-induced long QT syndrome, short stature, microcephaly, small ears, 2–3 cutaneous syndactyly[journals.plos.org]

  • De Hauwere Syndrome

    Cognitive and behavioral problems as well as developmental delay have been described.[aao.org] Nonocular features included characteristic facies (maxillary hypoplasia, short philtrum, and protruding lower lip of mild prognathism), dental anomalies (microdontia, hypodontia[genome.jp]

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