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Results 1 - 10 of 23 for Syndactyly type 1
  1. GJA1 gene 
    ... CONGENITAL ALOPECIA 1; PPKCA1 GAP JUNCTION PROTEIN, ALPHA-1; GJA1 SYNDACTYLY, TYPE III; SDTY3 NCBI Gene ClinVar Boyden LM, Craiglow ... correlates with the phenotype observed in oculodentodigital syndrome/type III syndactyly. J Med Genet. 2004 Jan;41(1):60-7. doi: 10.1136/jmg.2003.012005. ...
    https://medlineplus.gov/genetics/gene/gja1 - Genetics
  2. Pfeiffer syndrome 
    ... be some webbing or fusion between the digits (syndactyly).Pfeiffer syndrome is divided into three subtypes. Type 1, also known as classic Pfeiffer syndrome, has symptoms ...
    https://medlineplus.gov/genetics/condition/pfeiffer-syndrome - Genetics
  3. Guide to Understanding Pfeiffer Syndrome (Children's Craniofacial Association) - PDF  
    Craniofacial Abnormalities/Specifics ... Craniofacial Abnormalities ... Children's Craniofacial Association ... PDF
    https://ccakids.org/.../uploads/2022/01/pfeiffer-guide_2018.pdf - External Health Links
  4. Klippel-Trenaunay syndrome 
    ... complications of Klippel-Trenaunay syndrome can include a type of skin infection called cellulitis, ... Klippel-Trenaunay syndrome ...
    https://medlineplus.gov/.../condition/klippel-trenaunay-syndrome - Genetics
  5. Feingold syndrome 
    ... among affected individuals.Individuals with Feingold syndrome type 1 or type ... hypoplasia), and fusion (syndactyly) of the second and third toes or the ...
    https://medlineplus.gov/genetics/condition/feingold-syndrome - Genetics
  6. NOG gene 
    ... features like those seen in multiple synostoses syndrome 1.Brachydactyly type B2 ... or toes (syndactyly).As in tarsal-carpal coalition syndrome, the NOG ...
    https://medlineplus.gov/genetics/gene/nog - Genetics
  7. Oral-facial-digital syndrome 
    ... Registry: Orofaciodigital syndrome VIII Orofaciodigital syndrome Orofaciodigital syndrome type 1 Orofaciodigital syndrome type 2 National Organization for Rare ...
    https://medlineplus.gov/.../condition/oral-facial-digital-syndrome - Genetics
  8. Nager syndrome 
    ... cause in these families is unknown. Acrofacial dysostosis 1, Nager type AFD1 NAFD Nager acrofacial dysostosis Nager acrofacial dysostosis ... for Rare Disorders (NORD) ClinicalTrials.gov ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1 PubMed Bernier FP, Caluseriu O, Ng S, ...
    https://medlineplus.gov/genetics/condition/nager-syndrome - Genetics
  9. Andersen-Tawil syndrome 
    ... mutations in this gene, it is classified as type 1 (ATS1).The KCNJ2 gene provides instructions for making ...
    https://medlineplus.gov/genetics/condition/andersen-tawil-syndrome - Genetics
  10. Timothy syndrome 
    ... new form of long QT syndrome associated with syndactyly. J Am Coll Cardiol. 1995 Jan;25(1):59-64. doi: 10.1016/0735-1097(94) ...
    https://medlineplus.gov/genetics/condition/timothy-syndrome - Genetics
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