Robinow syndrome is a rare disorder that affects the development of many parts of the body, particularly the bones. Researchers have identified two major ...
Important It is possible that the main title of the report Robinow Syndrome is not the name you expected. Please check the synonyms listing to find the ...
Robinow syndrome is an extremely rare genetic disorder characterized by short-limbed dwarfism, abnormalities in the head, face, and external genitalia, as well as ...
1. J Med Genet. 2002 May;39(5):305-10. Robinow syndrome. Patton MA(1), Afzal AR. Author information: (1)Department of Medical Genetics, St George's ...
The Robinow Syndrome Foundation We are a "little" group of families reaching out for one anothers support on dealing with this medical rarity and how it affects all ...
Robinow Syndrome information including symptoms, diagnosis, misdiagnosis, treatment, causes, patient stories, videos, forums, prevention, and prognosis.
Robinow syndrome is a rare autosomal recessive mesomelic dwarfism with just more than 100 cases reported in the literature so far. The lower extremity is spared with ...
Summary. Robinow syndrome (RS) is a rare genetic syndrome characterized by limb shortening and abnormalities of the head, face and external genitalia.
Robinow syndrome is an extremely rare inherited disorder characterized by mild to moderate short stature due to growth delays after birth (postnatal growth ...
General Discussion. Robinow syndrome is an extremely rare inherited disorder characterized by mild to moderate short stature due to growth delays after birth ...