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),...
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mathematician Van der Woude syndrome, congenital disorder first described in 1954 by American physician Anne Van der Woude (?–?) 5916 van der Woude, main-belt...
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List of diseases (V) (section Vac–Van)
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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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...
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syndrome VACTERL association Valentino's syndrome Van der Woude syndrome van Gogh syndrome Van Wyk and Grumbach syndrome Vanishing bile duct syndrome...
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Rett-like syndromes. Pitt-Hopkins syndrome is clinically similar to Angelman syndrome, Rett-syndrome, Mowat Wilson syndrome, and ATR-X syndrome. As more...
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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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Cleft lip and cleft palate (redirect from Cleft lip/palate syndrome 3)
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...
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Campomelic dysplasia (redirect from Camptomelic syndrome)
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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Craniofacial cleft (redirect from Van der Meulen classification)
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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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...
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syndrome Ulnar–mammary syndrome Van Der Woude syndrome Von Hippel–Lindau syndrome Watson syndrome Werner syndrome (adult progeria) Westerhof syndrome...
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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...
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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...
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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...
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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"...
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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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Gerodermia osteodysplastica (redirect from Martsolf Reed Hunter syndrome)
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"...
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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"...
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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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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...
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