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101 Possible Causes for Pediatric Disorder, Relative Prognathism

  • Smith-Magenis Syndrome

    Abstract Smith-Magenis Syndrome (SMS) is a complex, pediatric, neurobehavioral, contiguous gene syndrome ascribed to interstitial microdeletion of chromosome 17, band 11.2[] Infants are described as looking "cherubic" with a Down syndrome-like appearance, whereas with age the facial appearance is that of relative prognathism.[] Facial dysmorphisms include broad and square-shaped face, mild face hypoplasia, brachicephaly, short nasal philtrum, a tendency toward an everted upper lip, and relative prognathism[]

  • Cleidocranial Dysplasia

    Tachdjian's Pediatric Orthopaedics. 5th ed. Philadelphia, PA: Elsevier Saunders; 2014:chap 40. Horton WA, Hecht JT. Disorders involving transcription factors.[] prognathic mandible (Pseudoprognathism),in addition to an unusual hypermobility of the shoulders ( Figure 1 ).[] The facial appearance was frontal bossing, mild hypertelorism, mid-face deficiency and relative mandibular prognathism. His intelligence was normal.[]

  • Osteogenesis Imperfecta

    Neurology and Musculoskeletal disorders and Home care, Astrid Lindgren Children's Hospital at Karolinska University Hospital, Stockholm, Sweden.[] These subjects very often show signs of restrained vertical dimension, flattened cranial base, relative prognathism, and more forward, counterclockwise mandibular growth ([] […] congenital disorders is caused by a glycine substitution in the procollagen molecule?[]

  • Frontonasal Dysplasia

    Radiology of syndromes and metabolic disorders. Pediatric Surgery. 2 nd ed. Chicago, IL: Year Book Medical; 1983. p. 235. [Figure 1] [Table 1][] […] mandibular prognathism Premature closure of one or more sutures of the skull 756.0 Excludes Applies To Absence of skull bones Acrocephaly Congenital deformity of forehead[] Pediatric Surgery. 2nd ed. Chicago, IL: Year Book Medical; 1983. Radiology of syndromes and metabolic disorders; p. 235. [ Google Scholar ][]

  • Simpson Dysmorphia Syndrome

    Turk J Pediatr 2010;52: 525-528.[] […] mandibular prognathism, shallow orbit Jackson-Weiss syndrome 123150 AD craniosynostosis, midfacial hypoplasia Apert syndrome 101200 AD craniosynostosis, brachysphenocephalic[] You’ll benefit from unique, global perspectives on adult and pediatric endocrinology prepared by an international team of renowned authorities.[]

  • Schwartz-Lelek Syndrome

    Craniotubular bone disorders. Pediatric Radiology, Vol. 24, Issue. 6, p. 392.[] The mandible has an open (obtuse) angle that causes relative prognathism.[] […] of Rio de Janeiro, emphasizing the importance of early diagnosis of this genetic disorder.[]

  • SHORT Syndrome

    Pediatric disorders of sex development. In: Melmed S, Polonsky KS, Larsen PR, Kronenberg HM, eds. Williams Textbook of Endocrinology. 13th ed.[] Other features can be hypoplasia of the malar bones, broad flat nasal root, prominent supraorbital ridges, relative prognathism, and mild telecanthus with or without hypertelorism[] Nelson textbook of pediatrics. 1. 20th ed. Philadelphia: Elsevier; 2016.p. 84-9. [ Links ] 5 Ergun-Longmire B, Wajnrajch MP. Growth and growth disorders.[]

  • Hereditary Hyperphosphatasia

    Bone Histomorphometry 383 Chapter 17 A Diagnostic Approach to Skeletal Dysplasias 403 Chapter 26 Familial Hypophosphatemia and Related Disorders 699 Chapter 27 Hereditary[] The mandible is prognathic, broadened and squared, and dental malocclusion is frequent [224]. The face may be distorted with relative midfacial hypo- 403 plasia.[] Osteoporosis 439 Chapter 19 Osteogenesis Imperfecta 511 Chapter 20 Sclerosing Bone Dysplasias 541 Chapter 21 Parathyroid Disorders 557 Chapter 22 Fibrous Dysplasia 589 Chapter[]

  • Acrocephaly

    Apply the latest treatment options in pediatric care with new chapters on pediatric sleep disorders, pediatric infectious disease, and evaluation and management of the infant[] If the alveolar process is recessed with the rest of the maxillary compound, the protrusion of the normally developed mandible (relative prognathism) adds another factor to[] There may be some features of Crouzon's disease associated with oxycephaly, The typical features of dysostosis craniofacialis are recession of maxilla with relative prognathism[]

  • Fetal Alcohol Syndrome

    Pediatric Feeding Disorders Program - Provides assessment and treatment for children who have difficulty eating related to food selectivity, food refusal, and disruptive mealtime[] Retrognathia in infancy, micrognathia or relative prognathism in adolescence and a low nasal bridge. Microphthalmia, strabismus, ptosis and short palpebral fissures.[] Updated clinical guidelines for diagnosing fetal alcohol spectrum disorders. Pediatrics. 2016;138(2). pii: e20154256 PMID: 27464676[]

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