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Results 1 - 7 of 7 for Symphalangism with multiple anomalies of hands feet
  1. Adams-Oliver syndrome 
    ... absence of hair growth in the affected area.Abnormalities of the hands and ... together (syndactyly), and abnormally short or missing fingers or toes ( ...
    https://medlineplus.gov/genetics/condition/adams-oliver-syndrome - Genetics
  2. NOG gene 
    ... of the bones in the ears (stapes fixation).Multiple synostoses syndrome 1 ... the bones in the hands, feet, hips, and upper part of the spine (cervical ...
    https://medlineplus.gov/genetics/gene/nog - Genetics
  3. Jackson-Weiss syndrome 
    ... skull, widely spaced eyes, and a bulging forehead.Foot abnormalities are the ... shaped. The hands are almost always normal.Some individuals with Jackson- ...
    https://medlineplus.gov/genetics/condition/jackson-weiss-syndrome - Genetics
  4. 22q13.3 deletion syndrome 
    ... seen with this condition include large and fleshy hands and/or feet, a fusion of the second and third toes (syndactyly), and small or abnormal toenails. Some affected individuals ...
    https://medlineplus.gov/genetics/condition/22q133-deletion-syndrome - Genetics
  5. Apert syndrome 
    ... moderate intellectual disability.Individuals with Apert syndrome have syndactyly of the fingers and toes. The severity of the fusion varies, although the hands tend to be more severely affected than the feet. Most commonly, three digits on each hand and ...
    https://medlineplus.gov/genetics/condition/apert-syndrome - Genetics
  6. Guide to Understanding Apert Syndrome (Children's Craniofacial Association) - PDF  
    Craniofacial Abnormalities/Specifics ... Craniofacial Abnormalities ... Children's Craniofacial Association ... PDF
    https://www.ccakids.org/assets/syndromebk_apert.pdf - External Health Links
  7. Pfeiffer syndrome 
    ... factor receptors 1 and 2, respectively. Among their multiple functions, these proteins signal immature cells to ... This condition is inherited in an ...
    https://medlineplus.gov/genetics/condition/pfeiffer-syndrome - Genetics