• Van der Woude syndrome (VDWS) is a genetic disorder characterized by the combination of lower lip pits, cleft lip with or without cleft palate (CL/P),...
    12 KB (1,579 words) - 19:58, 15 September 2024
  • mathematician Van der Woude syndrome, congenital disorder first described in 1954 by American physician Anne Van der Woude (?–?) 5916 van der Woude, main-belt...
    2 KB (214 words) - 18:27, 17 October 2024
  • Berghe–Dequeker syndrome Van Den Bosch syndrome Van Den Ende–Brunner syndrome Van der Woude syndrome Van der Woude syndrome 2 Van Goethem syndrome Van...
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  • Thumbnail for Popliteal pterygium syndrome
    anomalies, and fissure of the sacral vertebrae. Van der Woude syndrome (VDWS) and popliteal pterygium syndrome (PPS) are allelic variants of the same condition;...
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  • toes. Some common syndromes that involved phenotypic variability due to expressivity include: Marfan syndrome, Van der Woude Syndrome, and neurofibromatosis...
    16 KB (1,735 words) - 00:14, 9 October 2024
  • syndrome VACTERL association Valentino's syndrome Van der Woude syndrome van Gogh syndrome Van Wyk and Grumbach syndrome Vanishing bile duct syndrome...
    42 KB (4,068 words) - 16:56, 1 November 2024
  • Thumbnail for Pitt–Hopkins syndrome
    Rett-like syndromes. Pitt-Hopkins syndrome is clinically similar to Angelman syndrome, Rett-syndrome, Mowat Wilson syndrome, and ATR-X syndrome. As more...
    18 KB (1,866 words) - 00:27, 18 November 2024
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    the autosomal dominant van der Woude syndrome (VWS) or the related popliteal pterygium syndrome (PPS). Van der Woude syndrome can include cleft lip and...
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  • occur alone or in association with cleft lip and palate, termed Van der Woude syndrome. They are divided into three types based on their location: commissural...
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  • Thumbnail for Cleft lip and cleft palate
    in the HYAL2 gene and cleft lip and cleft palate formation. The Van der Woude syndrome is caused by a specific variation in the gene IRF6 that increases...
    92 KB (10,270 words) - 01:07, 15 November 2024
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    ACD/MPV FOXI1 Enlarged vestibular aqueduct FOXL2 Premature ovarian failure 3 FOXP3 IPEX 3.5 IRF6 Van der Woude syndrome Popliteal pterygium syndrome...
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  • regulatory factor 6 or, IRF6. Mutations in IRF6 cause Van der Woude syndrome, the most common clefting syndrome. Ventral anterior homeobox 1, VAX1, and noggin...
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  • disease, which causes tumours to grow on many parts of the body, Van der Woude syndrome, a form of cleft lip and palate, and for the hereditary skin condition...
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  • Thumbnail for Adebowale A. Adeyemo
    families with Van Der Woude syndrome and popliteal pterygium syndrome in Africa and helped identify rare functional variants in non-syndromic cleft lip/palate...
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    prostate cancer Stickler syndrome TAR syndrome trimethylaminuria Usher syndrome Usher syndrome type II Van der Woude syndrome Variegate porphyria G-banding...
    46 KB (3,290 words) - 20:16, 17 August 2024
  • Thumbnail for List of skin conditions
    syndrome Ulnar–mammary syndrome Van Der Woude syndrome Von Hippel–Lindau syndrome Watson syndrome Werner syndrome (adult progeria) Westerhof syndrome...
    198 KB (17,956 words) - 10:27, 2 November 2024
  • Thumbnail for Hantavirus hemorrhagic fever with renal syndrome
    36: 62–102. PMID 2573914. Muranyi, Walter; Bahr, Udo; Zeier, Martin; Van Der Woude, Fokko J. (2005). "Hantavirus Infection". Journal of the American Society...
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    alpha gene also cause branchio-oculo-facial syndrome, which has overlapping features with Van der Woude syndrome such as orofacial clefting and occasional...
    24 KB (3,050 words) - 06:21, 2 January 2024
  • Thumbnail for Grainyhead-like gene family
    that causes an increase or a decrease in expression, can lead to Van der Woude syndrome, which is characterized by phenotypes that include cleft lip and/or...
    31 KB (3,243 words) - 07:56, 2 November 2024
  • Thumbnail for C1orf74
    palate and Van der Woude syndrome. Mutations in regions upstream and downstream of IRF6, such as C1orf74, may also result in Van der Woude syndrome or these...
    9 KB (870 words) - 04:31, 14 March 2022
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    Dixon MJ, Murray JC (January 2000). "A preliminary gene map for the Van der Woude syndrome critical region derived from 900 kb of genomic sequence at 1q32-q41"...
    11 KB (1,336 words) - 01:57, 2 November 2024
  • Thumbnail for Lillian Glass
    Speech-Language Pathologists's Role in Understanding the Genetics of Van Der Woude Syndrome". Journal of Speech and Hearing Disorders. 44 (4): 472–478. doi:10...
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    syndrome WDR61 SKI8; REC14 80349 WDR62 MCPH2; C19orf14 284403 microcephaly WDR63 DIC3; NYD-SP29 126820 WDR64 128025 WDR65 CFAP57; VWS2 149465 Van der...
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    human TAX-1 gene to 1q32.1: a region implicated in microcephaly and Van der Woude syndrome" (PDF). Human Molecular Genetics. 2 (9): 1461–2. doi:10.1093/hmg/2...
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  • therapy Related syndromes Hearing loss with craniofacial syndromes Pierre Robin syndrome Popliteal pterygium syndrome Van der Woude syndrome National and...
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    Hennekam, Raoul C. M; Van Den Boogaard, Marie-Jose; Sibbles, Barbara J.; Van Spijker, Hilda G. (2005-06-06). "Rubinstein-Taybi syndrome in the Netherlands"...
    14 KB (1,449 words) - 16:00, 10 October 2024
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    Y, Dixon MJ, Murray JC (2000). "A preliminary gene map for the Van der Woude syndrome critical region derived from 900 kb of genomic sequence at 1q32-q41"...
    9 KB (1,182 words) - 11:51, 2 November 2024
  • therapy Related syndromes Hearing loss with craniofacial syndromes Pierre Robin syndrome Popliteal pterygium syndrome Van der Woude syndrome National and...
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  • disease; 239100; SOST van Buchem disease, type 2; 607636; LRP5 van der Woude syndrome; 119300; IRF6 Vasculopathy, retinal, with cerebral leukodystrophy;...
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    "No Wise King without a Wise Woman (I Kings III 16–28)", in A. S. van der Woude (ed.), New Avenues in the Study of the Old Testament: A Collection of...
    49 KB (6,687 words) - 20:28, 17 November 2024