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Robinow syndrome
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- 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 ...
- ... 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 ...
- ... 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 ...
- ... 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 ...
- ... 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 ...
- ... 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 ...
- ... 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 ...