951 Possible Causes for LEOPARD Syndrome

  • Hypertelorism

    Hypertelorism can also be seen in Apert syndrome, craniofrontonasal dysplasia, Noonan syndrome, neurofibromatosis, LEOPARD syndrome, Crouzon syndrome, Wolf-Hirschhorn syndrome[facecorrection.com] Neurosurgery (1991) [ Pubmed ] Leopard syndrome. Tong, K.L., Ding, Z.P., Chua, T.[wikigenes.org] 13 Interstitial deletion of chromosome 17 Isolated occurrence LEOPARD syndrome Loeys-Dietz syndrome Median cleft face Megalencephaly Meningoencephalocele Noonan syndrome[rightdiagnosis.com]

  • Hearing Impairment
  • Cardiac Arrhythmia
  • Acute Myelomonocytic Leukemia

    Leukemia has not previously been reported in patients with LEOPARD syndrome .[journals.lww.com] A missense mutation (836 G; Tyr279Cys) in exon 7 of PTPN11 gene was identified in this patient and his mother with LEOPARD syndrome .[journals.lww.com] […] doi: 10.1097/01.mph.0000199590.21797.0b Original Articles Abstract Author Information The LEOPARD syndrome is a complex of multisystemic congenital abnormalities characterized[journals.lww.com]

  • Wolff-Parkinson-White Syndrome

    LEOPARD syndrome with Wolff-Parkinson-White syndrome on electrocardiography.[ijdvl.com] LEOPARD syndrome with Wolff-Parkinson-White syndrome on electrocardiography. Indian J Dermatol Venereol Leprol[ijdvl.com] LEOPARD syndrome with Wolff-Parkinson-White syndrome on electrocardiography 1 Department of Skin and Veneral Diseases, Post Graduate Institute of Medical Sciences, Rohtak,[ijdvl.com]

  • LEOPARD Syndrome

    […] is LEOPARD Syndrome?[dovemed.com] PMID 15520399 PTPN11 mutations in LEOPARD syndrome.[atlasgeneticsoncology.org] There are three types of LEOPARD syndrome, which are distinguished by their underlying genetic cause. [diseaseinfosearch.org]

  • LEOPARD Syndrome

    PMID 15520399 PTPN11 mutations in LEOPARD syndrome.[atlasgeneticsoncology.org] LEOPARD syndrome An autosomal dominant [MIM 151100] condition with thousands of 1–5-mm darkly pigmented macules on the skin leopard syndrome Multiple lentigines syndrome An[medical-dictionary.thefreedictionary.com] Eysenbach) synonyms LEOPARD Syndrome, Lentiginosis Syndrome UMLS Generalised lentiginosis, Generalized lentiginosis, LEOPARD syndrome, Leopard syndrome lentiginosis, Multiple[dermis.net]

  • Noonan Syndrome with Multiple Lentigines

    PMID 15520399 PTPN11 mutations in LEOPARD syndrome.[atlasgeneticsoncology.org] Leopard syndrome The RAS opathies HEREDITY The inheritance pattern of LEOPARD syndrome is autosomal dominant .[flipper.diff.org] […] looked like in kids with LEOPARD Syndrome.”[blog.laurenshope.com]

  • Turner Syndrome

    LEOPARD SYNDROME , a disorder that has clinical features overlapping those of Noonan Syndrome, is also due to mutations in PTPN11.[hon.ch] Synonym(s): Male Turner Syndrome / Turner Syndrome, Male / Female Pseudo-Turner Syndrome / Turner's Syndrome, Male / More information from the Genetics Home Reference Website[hon.ch] In addition, there is a syndrome called neurofibromatosis-Noonan syndrome.[hon.ch]

  • Martinez-Frias Syndrome

    LEOPARD syndrome. Multiple lentigines. Hypertrophic cardiomyopathy. RAS-MAPK genes.[revespcardiol.org] ; CS, Costello syndrome; LS, LEOPARD syndrome; NA, not available; NCFCS, neurocardiofaciocutaneous syndromes; NE, not evaluable; NS, Noonan syndrome; SD, standard deviations[revespcardiol.org] Abstract Introduction and objectives LEOPARD syndrome is an autosomal dominant condition related to Noonan syndrome, although it occurs less frequently.[revespcardiol.org]

Further symptoms