Create issue ticket

1,425 Possible Causes for Crouzon Syndrome

  • Acanthosis Nigricans

    The 5% of individuals with Crouzon syndrome who have pigmentary changes in the skin are said to have Crouzon syndrome with acanthosis nigricans (CAN).[ncbi.nlm.nih.gov] CONCLUSIONS AND RELEVANCE: In addition to craniofacial malformations, Crouzon syndrome with acanthosis nigricans results in characteristic cutaneous findings.[ncbi.nlm.nih.gov] Crouzon syndrome with acanthosis nigricans (CAN) is caused by a mutation in the fibroblast growth factor receptor ( FGFR) 3 gene that presents clinically as Crouzonoid craniofacial[ncbi.nlm.nih.gov]

  • Autosomal Dominant Prognathism

    A case of Crouzon syndrome is presented here.[mjdrdypu.org] Crouzon syndrome: A comprehensive review and case report.[jdrntruhs.org] This syndrome is named after Octave Crouzon, Crouzon syndrome on Genetics Home Reference from U.S.[en.wikipedia.org]

  • Crouzon Syndrome

    People with Crouzon syndrome are usually of normal intelligence. Crouzon syndrome is seen in about 16 per million newborns.[ghr.nlm.nih.gov] Apert syndrome Treacher Collins syndrome Hearing loss with craniofacial syndromes Crouzon syndrome on Genetics Home Reference from U.S.[en.wikipedia.org] Crouzon syndrome is a rare genetic disorder characterized by distinctive malformations of the skull and facial region.[ncbi.nlm.nih.gov]

  • Craniosynostosis

    The craniofacial features in this case were in keeping with a diagnosis of Crouzon syndrome which was confirmed by molecular testing of the FGFR2 gene.[ncbi.nlm.nih.gov] […] which, however, may also occur in some cases of Crouzon syndrome.[ncbi.nlm.nih.gov] Infants with Apert syndrome also face greater developmental impairments than those with Crouzon syndrome [9].[eyewiki.aao.org]

  • Familial Scaphocephaly Syndrome

    Familial Crouzon syndrome.[contempclindent.org] Patient Information - Crouzon Syndrome CROUZON syndrome is an inherited syndrome of Craniofacial Dysmorphology or abnormal craniofacial appearance, which was originally described[headlines.org.uk] Crouzon disease. Orphanet Encyclopedia, November 2013. Available at: Accessed September 20, 2016. Genetics Home Reference website. Crouzon syndrome. February 2008.[rarediseases.org]

  • Cloverleaf Skull

    syndrome.[fn.bmj.com] Petero suffers from a rare genetic disorder known as Crouzon's Syndrome or Crouzon's Disease.[kemiamusa.blogspot.com] Synonyms of Crouzon Syndrome Craniofacial Dysostosis Craniostenosis, Crouzon Type Crouzon Craniofacial Dysostosis General Discussion Summary Crouzon syndrome is a rare genetic[rarediseases.org]

  • Acrocephaly

    No physiological spinal curvature is observed in Crouzon syndrome. Short stature and dark skin of Crouzon syndrome. Koilosternia rarely occurs. Skin usually is dark.[emedicine.medscape.com] Differential diagnosis Oxycephaly may also be a feature of certain syndromes (Crouzon syndrome and Pfeiffer syndrome; see these terms).[orpha.net] We initially suspected a cranyosinostosis due to a Crouzon syndrome or SCS.[degruyter.com]

  • Craniosytosis Type 4

    Crouzon syndrome MedGen UID: 1162 • Concept ID: C0010273 • Disease or Syndrome Crouzon syndrome is a genetic disorder characterized by the premature fusion of certain skull[ncbi.nlm.nih.gov] Infants with Apert syndrome also face greater developmental impairments than those with Crouzon syndrome [9].[eyewiki.aao.org] Figure 30-11 A 19-year-old boy who was born with Crouzon syndrome.[pocketdentistry.com]

  • Craniosynostosis Type 3

    […] rare craniofacial clefts, acute and chronic sequellae of facial fractures, cleft lip and palate, micrognathia, Treacher Collins Syndrome, Apert's Syndrome, Crouzon's Syndrome[aomsi.com] Crouzon syndrome: AD Apert's syndrome: AD Pfeiffer syndrome: AD Saethre-Chotzen syndrome: AD Carpenter syndrome: AR Features of Crouzon syndrome -Most common form of syndromic[quizlet.com] In contrast to Crouzon syndrome, craniofacial involvement is apparent at birth.[rrnursingschool.biz]

  • Isolated Trigonocephaly

    Infants with Apert syndrome also face greater developmental impairments than those with Crouzon syndrome [9].[eyewiki.aao.org] There is evidence of FGFR2 mutation in Apert Syndrome, FGFR3 in Crouzon syndrome and FGFR1 in Pfeiffer syndrome.[childneurosurgeon.com] In contrast to Crouzon syndrome, craniofacial involvement is apparent at birth.[rrnursingschool.biz]

Further symptoms