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Results 1 - 9 of 9 for Robinow syndrome
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  1. Robinow syndrome 
    Robinow syndrome is a rare disorder that affects the development of many parts of the body, particularly the skeleton. The types of Robinow syndrome can be distinguished by the severity of their ...
    https://medlineplus.gov/genetics/condition/robinow-syndrome - Genetics
  2. ROR2 gene 
    ... found to cause the autosomal recessive form of Robinow syndrome, a condition that affects the development of many ... changes lead to the skeletal abnormalities characteristic of Robinow syndrome. A lack of this protein during early development ...
    https://medlineplus.gov/genetics/gene/ror2 - Genetics
  3. DVL1 gene 
    ... found to cause the autosomal dominant form of Robinow syndrome, a condition that affects the development of many ... mutations underlie a variant type of autosomal dominant Robinow syndrome called the osteosclerotic form, which features increased bone ...
    https://medlineplus.gov/genetics/gene/dvl1 - Genetics
  4. WNT5A gene 
    ... found to cause the autosomal dominant form of Robinow syndrome, a condition that affects the development of many ... organs and tissues, leading to the features of Robinow syndrome. More About This Health Condition hWNT5A wingless-type ...
    https://medlineplus.gov/genetics/gene/wnt5a - Genetics
  5. FZD2 gene 
    ... gene have been found to cause autosomal dominant Robinow syndrome, a condition that affects the development of many ... it actually represents a subtype of autosomal dominant Robinow syndrome.Three of the known mutations change a single ...
    https://medlineplus.gov/genetics/gene/fzd2 - Genetics
  6. DVL3 gene 
    ... found to cause the autosomal dominant form of Robinow syndrome, a condition that affects the development of many ... many organs and tissues before birth, leading to Robinow syndrome. More About This Health Condition dishevelled 3 (homologous ...
    https://medlineplus.gov/genetics/gene/dvl3 - Genetics
  7. Saethre-Chotzen syndrome 
    ... spine (the vertebra), hearing loss, and heart defects.Robinow-Sorauf syndrome is a condition with features similar to those ... Dysostosis craniofacialis with hypertelorism SCS Genetic Testing Registry: Robinow-Sorauf syndrome Genetic Testing Registry: Saethre-Chotzen syndrome Saethre-Chotzen ...
    https://medlineplus.gov/genetics/condition/saethre-chotzen-syndrome - Genetics
  8. Craniofacial Abnormalities (National Library of Medicine)  
    Craniofacial is a medical term that relates to the bones of the skull and face. Craniofacial abnormalities are birth defects of the face or head. Some, like cleft ...
    https://medlineplus.gov/craniofacialabnormalities.html - Health Topics
  9. Dwarfism (National Library of Medicine)  
    People with dwarfism have short stature. This means that their height is under 4' 10" as an adult. They are usually of normal intelligence. Dwarfism most often ...
    https://medlineplus.gov/dwarfism.html - Health Topics