1,260 Possible Causes for LEOPARD Syndrome in USA

  • LEOPARD Syndrome

    What are the Causes of LEOPARD Syndrome? … What are the Signs and Symptoms of LEOPARD Syndrome? … What are the possible Complications of LEOPARD Syndrome?[1]

  • Costello Syndrome

    [Gelb BD, Tartaglia M, for GeneReviews for LEOPARD syndrome, 2010] External Website Links: GeneReviews for LEOPARD syndrome Genetic Home Reference for Multiple lentigines … syndrome Mutations: PTPN11, RAF1 Noonan syndrome with multiple lentigenes (NSML) is also known as LEOPARD syndrome (LS) is an acronym for the cardinal features l entigines … syndrome (CFCS) Costello syndrome (CS) Neurofibromatosis type 1 (NF1) Noonan Syndromes Noonan syndrome (NS) Legius syndrome (LS) Noonan syndrome with Multiple Lentigenes (NSML)/LEOPARD[2]

  • Moynahan Syndrome

    Noonan syndrome with multiple lentigines (NSML) (also known as LEOPARD syndrome, cardiocutaneous syndrome, Gorlin syndrome II, lentiginosis profusa syndrome, progressive cardiomyopathic … An alternative name of the condition, LEOPARD syndrome, is a mnemonic, originally coined in 1969, as the condition is characterized by some of the following seven conditions[3]

  • Pulmonary Valve Stenosis

    Noonan Syndrome with Multiple Lentigines (LEOPARD Syndrome); Tetralogy of Fallot; Williams-Beuren Syndrome Q22.1 Congenital pulmonary valve stenosis I37.0 Nonrheumatic pulmonary[4]

  • Neurofibromatosis Type 1

    The diagnosis of neurofibromatosis is done via the following means: Conditions which may be confused with NF include, LEOPARD syndrome, and Legius syndrome.[5]

  • Neurofibromatosis Type 2

    The diagnosis of neurofibromatosis is done via the following means: Conditions which may be confused with NF include, LEOPARD syndrome, and Legius syndrome.[6]

  • Kabuki Syndrome

    dysplasi (CED, Sensenbrenner syndrom) • Kulde-indusert svettesyndrom (CISS1) • Kulde-indusert svettesyndrom (CISS2) • Langer Giedeon syndrom • Larsen syndrom • Legius syndrom • Leopardsyndrom • Lissencephaly type 1 • Loeys-Dietz syndrom • Marfan syndrom • Meckel syndrom • Mental retardasjon • Mental retardasjon, X-bundet, ARX-relatert • Mikrodelesjonssyndromer[7]

  • Gorlin Syndrome

    Alternative eponyms Capute-Rimoin-Konigsmark-Esterly-Richardson syndrome LEOPARD syndrome Leopard skin syndrome Moynahan syndrome Related people Arnold J.[8]

  • Hypertelorism
    LEOPARD Syndrome

    Hypertelorism can also be seen in Apert syndrome, craniofrontonasal dysplasia, Noonan syndrome, neurofibromatosis, LEOPARD syndrome, Crouzon syndrome, Wolf–Hirschhorn syndrome[9]

  • Alagille Syndrome

    dysplasi (CED, Sensenbrenner syndrom) • Kulde-indusert svettesyndrom (CISS1) • Kulde-indusert svettesyndrom (CISS2) • Langer Giedeon syndrom • Larsen syndrom • Legius syndrom • Leopardsyndrom • Lissencephaly type 1 • Loeys-Dietz syndrom • Marfan syndrom • Meckel syndrom • Mental retardasjon • Mental retardasjon, X-bundet, ARX-relatert • Mikrodelesjonssyndromer … vascular system abnormalities are seen in isolation as well as in syndromes such as Noonan syndrome , Watson syndrome (pulmonic stenosis and neurofibromatosis type 1 ), LEOPARD[10] [11]

Further symptoms

Similar symptoms

References

  1. LEOPARD Syndrome, http://www.dovemed.com/diseases-conditions/leop…
  2. Syndromes - The RASopathies Network, https://rasopathiesnet.org/rasopathies/syndromes/
  3. Noonan syndrome with multiple lentigines, https://en.wikipedia.org/wiki/Noonan_syndrome_w…
  4. Pulmonary Valve Stenosis | Diseases & Conditions, http://5minuteconsult.com/collectioncontent/1-1…
  5. Neurofibromatosis, https://en.wikipedia.org/wiki/Neurofibromatosis
  6. Neurofibromatosis, https://en.wikipedia.org/wiki/Neurofibromatosis
  7. Kabuki syndrom: Syndromer | Norsk portal for medisinsk-genetiske analyser, https://www.genetikkportalen.no/?act=tilst&TgID…
  8. Whonamedit - dictionary of medical eponyms, http://www.whonamedit.com/synd.cfm/2212.html
  9. Hypertelorism, https://en.wikipedia.org/wiki/Hypertelorism
  10. Alagille Syndrome - GeneReviews® - NCBI Bookshelf, https://www.ncbi.nlm.nih.gov/books/NBK1273/
  11. Alagille syndrom: Syndromer | Norsk portal for medisinsk-genetiske analyser, https://www.genetikkportalen.no/?act=tilst&TgID…